Canonical Allele Identifier: CA401850607
Gene: LAMA1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.7015819T>G , CM000680.2:g.7015819T>G GRCh38
NC_000018.9:g.7015818T>G , CM000680.1:g.7015818T>G GRCh37
NC_000018.8:g.7005818T>G NCBI36
NG_034251.1:g.106996A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000389658.4:c.3029A>C MANE Select ENSP00000374309.3:p.Glu1010Ala
ENST00000389658.3:c.3029A>C ENSP00000374309.3:p.Glu1010Ala
ENST00000579014.5:n.4044A>C
NM_005559.3:c.3029A>C NP_005550.2:p.Glu1010Ala
XM_011525655.1:c.3029A>C XP_011523957.1:p.Glu1010Ala
XM_011525656.1:c.1457A>C XP_011523958.1:p.Glu486Ala
XM_011525657.1:c.3029A>C XP_011523959.1:p.Glu1010Ala
XM_011525655.2:c.3029A>C XP_011523957.1:p.Glu1010Ala
XM_011525656.2:c.1457A>C XP_011523958.1:p.Glu486Ala
NM_005559.4:c.3029A>C MANE Select NP_005550.2:p.Glu1010Ala