Canonical Allele Identifier: CA3992635
Gene: LAMA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 642364
dbSNP Id: rs763484341

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.129190231T>A , CM000668.2:g.129190231T>A GRCh38
NC_000006.11:g.129511376T>A , CM000668.1:g.129511376T>A GRCh37
NC_000006.10:g.129553069T>A NCBI36
NG_008678.1:g.312091T>A , LRG_409:g.312091T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000617695.5:c.1494T>A ENSP00000481744.2:p.Ser498Arg
ENST00000618192.5:c.1494T>A ENSP00000480802.2:p.Ser498Arg
ENST00000686599.1:n.1599T>A
ENST00000690881.1:n.957T>A
ENST00000421865.3:c.1494T>A MANE Select ENSP00000400365.2:p.Ser498Arg
ENST00000421865.2:c.1494T>A ENSP00000400365.2:p.Ser498Arg
ENST00000617695.4:c.1494T>A ENSP00000481744.1:p.Ser498Arg
ENST00000618192.4:c.1494T>A ENSP00000480802.1:p.Ser498Arg
NM_000426.3:c.1494T>A , LRG_409t1:c.1494T>A NP_000417.2:p.Ser498Arg
NM_001079823.1:c.1494T>A NP_001073291.1:p.Ser498Arg
XM_005266981.2:c.1494T>A XP_005267038.1:p.Ser498Arg
XM_005266982.2:c.1494T>A XP_005267039.1:p.Ser498Arg
XM_011535820.1:c.1494T>A XP_011534122.1:p.Ser498Arg
XM_005266981.3:c.1494T>A XP_005267038.1:p.Ser498Arg
XM_005266982.3:c.1494T>A XP_005267039.1:p.Ser498Arg
XM_011535820.2:c.1494T>A XP_011534122.1:p.Ser498Arg
XM_017010851.2:c.1500T>A XP_016866340.1:p.Ser500Arg
XM_017010853.1:c.1494T>A XP_016866342.1:p.Ser498Arg
NM_000426.4:c.1494T>A MANE Select NP_000417.3:p.Ser498Arg
NM_001079823.2:c.1494T>A NP_001073291.2:p.Ser498Arg