Canonical Allele Identifier: CA402063155
Gene: LAMA3 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.23928181G>A , CM000680.2:g.23928181G>A GRCh38
NC_000018.9:g.21508145G>A , CM000680.1:g.21508145G>A GRCh37
NC_000018.8:g.19762143G>A NCBI36
NG_007853.2:g.243584G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000269217.11:c.3409G>A MANE Plus Clinical ENSP00000269217.5:p.Gly1137Ser
ENST00000313654.14:c.8236G>A MANE Select ENSP00000324532.8:p.Gly2746Ser
ENST00000649721.1:c.4831G>A ENSP00000497885.1:p.Gly1611Ser
ENST00000269217.10:c.3409G>A ENSP00000269217.5:p.Gly1137Ser
ENST00000313654.13:c.8236G>A ENSP00000324532.8:p.Gly2746Ser
ENST00000399516.7:c.8068G>A ENSP00000382432.2:p.Gly2690Ser
ENST00000586751.5:c.3014G>A
ENST00000587184.5:c.3241G>A ENSP00000466557.1:p.Gly1081Ser
ENST00000588770.5:n.2814G>A
NM_000227.4:c.3409G>A NP_000218.3:p.Gly1137Ser
NM_001127717.2:c.8068G>A NP_001121189.2:p.Gly2690Ser
NM_001127718.2:c.3241G>A NP_001121190.2:p.Gly1081Ser
NM_198129.2:c.8236G>A NP_937762.2:p.Gly2746Ser
XM_011525978.1:c.8263G>A XP_011524280.1:p.Gly2755Ser
XM_011525979.1:c.8254G>A XP_011524281.1:p.Gly2752Ser
XM_011525980.1:c.8245G>A XP_011524282.1:p.Gly2749Ser
XM_011525981.1:c.8131G>A XP_011524283.1:p.Gly2711Ser
XM_011525982.1:c.7966G>A XP_011524284.1:p.Gly2656Ser
XM_011525978.2:c.8263G>A XP_011524280.1:p.Gly2755Ser
XM_011525979.2:c.8254G>A XP_011524281.1:p.Gly2752Ser
XM_011525980.2:c.8245G>A XP_011524282.1:p.Gly2749Ser
XM_011525981.2:c.8131G>A XP_011524283.1:p.Gly2711Ser
XM_011525982.2:c.7966G>A XP_011524284.1:p.Gly2656Ser
XM_017025743.1:c.6115G>A XP_016881232.1:p.Gly2039Ser
XM_017025744.1:c.3805G>A XP_016881233.1:p.Gly1269Ser
XR_001753199.1:n.8504G>A
NM_000227.5:c.3409G>A NP_000218.3:p.Gly1137Ser
NM_001127717.3:c.8068G>A NP_001121189.2:p.Gly2690Ser
NM_001127718.3:c.3241G>A NP_001121190.2:p.Gly1081Ser
NM_198129.3:c.8236G>A NP_937762.2:p.Gly2746Ser
NM_000227.6:c.3409G>A MANE Plus Clinical NP_000218.3:p.Gly1137Ser
NM_001127717.4:c.8068G>A NP_001121189.2:p.Gly2690Ser
NM_001127718.4:c.3241G>A NP_001121190.2:p.Gly1081Ser
NM_198129.4:c.8236G>A MANE Select NP_937762.2:p.Gly2746Ser