Canonical Allele Identifier: CA2290334567
Gene: LAMA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23928078_23928098delinsGCCTGACATGATCCATCTCTT , CM000680.2:g.23928078_23928098delinsGCCTGACATGATCCATCTCTT GRCh38
NC_000018.9:g.21508042_21508062delinsGCCTGACATGATCCATCTCTT , CM000680.1:g.21508042_21508062delinsGCCTGACATGATCCATCTCTT GRCh37
NC_000018.8:g.19762040_19762060delinsGCCTGACATGATCCATCTCTT NCBI36
NG_007853.2:g.243481_243501delinsGCCTGACATGATCCATCTCTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000269217.11:c.3351-45_3351-25delinsGCCTGACATGATCCATCTCTT MANE Plus Clinical ENSP00000269217.5:n.3351-45_3351-25delinsGCCTGACATGATCCATCTCT...
ENST00000313654.14:c.8178-45_8178-25delinsGCCTGACATGATCCATCTCTT MANE Select ENSP00000324532.8:n.8178-45_8178-25delinsGCCTGACATGATCCATCTCT...
ENST00000649721.1:c.4773-45_4773-25delinsGCCTGACATGATCCATCTCTT ENSP00000497885.1:n.4773-45_4773-25delinsGCCTGACATGATCCATCTCT...
ENST00000269217.10:c.3351-45_3351-25delinsGCCTGACATGATCCATCTCTT ENSP00000269217.5:n.3351-45_3351-25delinsGCCTGACATGATCCATCTCT...
ENST00000313654.13:c.8178-45_8178-25delinsGCCTGACATGATCCATCTCTT ENSP00000324532.8:n.8178-45_8178-25delinsGCCTGACATGATCCATCTCT...
ENST00000399516.7:c.8010-45_8010-25delinsGCCTGACATGATCCATCTCTT ENSP00000382432.2:n.8010-45_8010-25delinsGCCTGACATGATCCATCTCT...
ENST00000586751.5:c.2956-45_2956-25delinsGCCTGACATGATCCATCTCTT
ENST00000587184.5:c.3183-45_3183-25delinsGCCTGACATGATCCATCTCTT ENSP00000466557.1:n.3183-45_3183-25delinsGCCTGACATGATCCATCTCT...
ENST00000588770.5:n.2756-45_2756-25delinsGCCTGACATGATCCATCTCTT
NM_000227.4:c.3351-45_3351-25delinsGCCTGACATGATCCATCTCTT NP_000218.3:n.3351-45_3351-25delinsGCCTGACATGATCCATCTCTT
NM_001127717.2:c.8010-45_8010-25delinsGCCTGACATGATCCATCTCTT NP_001121189.2:n.8010-45_8010-25delinsGCCTGACATGATCCATCTCTT
NM_001127718.2:c.3183-45_3183-25delinsGCCTGACATGATCCATCTCTT NP_001121190.2:n.3183-45_3183-25delinsGCCTGACATGATCCATCTCTT
NM_198129.2:c.8178-45_8178-25delinsGCCTGACATGATCCATCTCTT NP_937762.2:n.8178-45_8178-25delinsGCCTGACATGATCCATCTCTT
XM_011525978.1:c.8205-45_8205-25delinsGCCTGACATGATCCATCTCTT XP_011524280.1:n.8205-45_8205-25delinsGCCTGACATGATCCATCTCTT
XM_011525979.1:c.8196-45_8196-25delinsGCCTGACATGATCCATCTCTT XP_011524281.1:n.8196-45_8196-25delinsGCCTGACATGATCCATCTCTT
XM_011525980.1:c.8187-45_8187-25delinsGCCTGACATGATCCATCTCTT XP_011524282.1:n.8187-45_8187-25delinsGCCTGACATGATCCATCTCTT
XM_011525981.1:c.8073-45_8073-25delinsGCCTGACATGATCCATCTCTT XP_011524283.1:n.8073-45_8073-25delinsGCCTGACATGATCCATCTCTT
XM_011525982.1:c.7908-45_7908-25delinsGCCTGACATGATCCATCTCTT XP_011524284.1:n.7908-45_7908-25delinsGCCTGACATGATCCATCTCTT
XM_011525978.2:c.8205-45_8205-25delinsGCCTGACATGATCCATCTCTT XP_011524280.1:n.8205-45_8205-25delinsGCCTGACATGATCCATCTCTT
XM_011525979.2:c.8196-45_8196-25delinsGCCTGACATGATCCATCTCTT XP_011524281.1:n.8196-45_8196-25delinsGCCTGACATGATCCATCTCTT
XM_011525980.2:c.8187-45_8187-25delinsGCCTGACATGATCCATCTCTT XP_011524282.1:n.8187-45_8187-25delinsGCCTGACATGATCCATCTCTT
XM_011525981.2:c.8073-45_8073-25delinsGCCTGACATGATCCATCTCTT XP_011524283.1:n.8073-45_8073-25delinsGCCTGACATGATCCATCTCTT
XM_011525982.2:c.7908-45_7908-25delinsGCCTGACATGATCCATCTCTT XP_011524284.1:n.7908-45_7908-25delinsGCCTGACATGATCCATCTCTT
XM_017025743.1:c.6057-45_6057-25delinsGCCTGACATGATCCATCTCTT XP_016881232.1:n.6057-45_6057-25delinsGCCTGACATGATCCATCTCTT
XM_017025744.1:c.3747-45_3747-25delinsGCCTGACATGATCCATCTCTT XP_016881233.1:n.3747-45_3747-25delinsGCCTGACATGATCCATCTCTT
XR_001753199.1:n.8446-45_8446-25delinsGCCTGACATGATCCATCTCTT
NM_000227.5:c.3351-45_3351-25delinsGCCTGACATGATCCATCTCTT NP_000218.3:n.3351-45_3351-25delinsGCCTGACATGATCCATCTCTT
NM_001127717.3:c.8010-45_8010-25delinsGCCTGACATGATCCATCTCTT NP_001121189.2:n.8010-45_8010-25delinsGCCTGACATGATCCATCTCTT
NM_001127718.3:c.3183-45_3183-25delinsGCCTGACATGATCCATCTCTT NP_001121190.2:n.3183-45_3183-25delinsGCCTGACATGATCCATCTCTT
NM_198129.3:c.8178-45_8178-25delinsGCCTGACATGATCCATCTCTT NP_937762.2:n.8178-45_8178-25delinsGCCTGACATGATCCATCTCTT
NM_000227.6:c.3351-45_3351-25delinsGCCTGACATGATCCATCTCTT MANE Plus Clinical NP_000218.3:n.3351-45_3351-25delinsGCCTGACATGATCCATCTCTT
NM_001127717.4:c.8010-45_8010-25delinsGCCTGACATGATCCATCTCTT NP_001121189.2:n.8010-45_8010-25delinsGCCTGACATGATCCATCTCTT
NM_001127718.4:c.3183-45_3183-25delinsGCCTGACATGATCCATCTCTT NP_001121190.2:n.3183-45_3183-25delinsGCCTGACATGATCCATCTCTT
NM_198129.4:c.8178-45_8178-25delinsGCCTGACATGATCCATCTCTT MANE Select NP_937762.2:n.8178-45_8178-25delinsGCCTGACATGATCCATCTCTT