Canonical Allele Identifier: CA2282694598
Gene: LAMA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.7015732A= , CM000680.2:g.7015732A= GRCh38
NC_000018.9:g.7015731A= , CM000680.1:g.7015731A= GRCh37
NC_000018.8:g.7005731A= NCBI36
NG_034251.1:g.107083T=

Transcript Alleles

HGVS Amino-acid change
ENST00000389658.4:c.3116T= MANE Select ENSP00000374309.3:p.Val1039=
ENST00000389658.3:c.3116T= ENSP00000374309.3:p.Val1039=
ENST00000579014.5:n.4131T=
NM_005559.3:c.3116T= NP_005550.2:p.Val1039=
XM_011525655.1:c.3116T= XP_011523957.1:p.Val1039=
XM_011525656.1:c.1544T= XP_011523958.1:p.Val515=
XM_011525657.1:c.3116T= XP_011523959.1:p.Val1039=
XM_011525655.2:c.3116T= XP_011523957.1:p.Val1039=
XM_011525656.2:c.1544T= XP_011523958.1:p.Val515=
NM_005559.4:c.3116T= MANE Select NP_005550.2:p.Val1039=