Canonical Allele Identifier: CA402051959
Gene: LAMA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23950070A>G , CM000680.2:g.23950070A>G GRCh38
NC_000018.9:g.21530034A>G , CM000680.1:g.21530034A>G GRCh37
NC_000018.8:g.19784032A>G NCBI36
NG_007853.2:g.265473A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000269217.11:c.4726A>G MANE Plus Clinical ENSP00000269217.5:p.Ser1576Gly
ENST00000313654.14:c.9553A>G MANE Select ENSP00000324532.8:p.Ser3185Gly
ENST00000649721.1:c.6148A>G ENSP00000497885.1:p.Ser2050Gly
ENST00000269217.10:c.4726A>G ENSP00000269217.5:p.Ser1576Gly
ENST00000313654.13:c.9553A>G ENSP00000324532.8:p.Ser3185Gly
ENST00000399516.7:c.9385A>G ENSP00000382432.2:p.Ser3129Gly
ENST00000587184.5:c.4558A>G ENSP00000466557.1:p.Ser1520Gly
ENST00000588004.1:c.74A>G
ENST00000588770.5:n.4131A>G
NM_000227.4:c.4726A>G NP_000218.3:p.Ser1576Gly
NM_001127717.2:c.9385A>G NP_001121189.2:p.Ser3129Gly
NM_001127718.2:c.4558A>G NP_001121190.2:p.Ser1520Gly
NM_198129.2:c.9553A>G NP_937762.2:p.Ser3185Gly
XM_011525978.1:c.9580A>G XP_011524280.1:p.Ser3194Gly
XM_011525979.1:c.9571A>G XP_011524281.1:p.Ser3191Gly
XM_011525980.1:c.9562A>G XP_011524282.1:p.Ser3188Gly
XM_011525981.1:c.9448A>G XP_011524283.1:p.Ser3150Gly
XM_011525982.1:c.9283A>G XP_011524284.1:p.Ser3095Gly
XM_011525978.2:c.9580A>G XP_011524280.1:p.Ser3194Gly
XM_011525979.2:c.9571A>G XP_011524281.1:p.Ser3191Gly
XM_011525980.2:c.9562A>G XP_011524282.1:p.Ser3188Gly
XM_011525981.2:c.9448A>G XP_011524283.1:p.Ser3150Gly
XM_011525982.2:c.9283A>G XP_011524284.1:p.Ser3095Gly
XM_017025743.1:c.7432A>G XP_016881232.1:p.Ser2478Gly
XM_017025744.1:c.5122A>G XP_016881233.1:p.Ser1708Gly
XR_001753199.1:n.9821A>G
NM_000227.5:c.4726A>G NP_000218.3:p.Ser1576Gly
NM_001127717.3:c.9385A>G NP_001121189.2:p.Ser3129Gly
NM_001127718.3:c.4558A>G NP_001121190.2:p.Ser1520Gly
NM_198129.3:c.9553A>G NP_937762.2:p.Ser3185Gly
NM_000227.6:c.4726A>G MANE Plus Clinical NP_000218.3:p.Ser1576Gly
NM_001127717.4:c.9385A>G NP_001121189.2:p.Ser3129Gly
NM_001127718.4:c.4558A>G NP_001121190.2:p.Ser1520Gly
NM_198129.4:c.9553A>G MANE Select NP_937762.2:p.Ser3185Gly