Canonical Allele Identifier: CA401850491

Gene: LAMA1

Linked Data

• MyVariant Identifiers: chr18:g.7015766T>G (hg19) ; chr18:g.7015767T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.7015767T>G , CM000680.2:g.7015767T>G	GRCh38
NC_000018.9:g.7015766T>G , CM000680.1:g.7015766T>G	GRCh37
NC_000018.8:g.7005766T>G	NCBI36
NG_034251.1:g.107048A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389658.4:c.3081A>C MANE Select	ENSP00000374309.3:p.Glu1027Asp
ENST00000389658.3:c.3081A>C	ENSP00000374309.3:p.Glu1027Asp
ENST00000579014.5:n.4096A>C
NM_005559.3:c.3081A>C	NP_005550.2:p.Glu1027Asp
XM_011525655.1:c.3081A>C	XP_011523957.1:p.Glu1027Asp
XM_011525656.1:c.1509A>C	XP_011523958.1:p.Glu503Asp
XM_011525657.1:c.3081A>C	XP_011523959.1:p.Glu1027Asp
XM_011525655.2:c.3081A>C	XP_011523957.1:p.Glu1027Asp
XM_011525656.2:c.1509A>C	XP_011523958.1:p.Glu503Asp
NM_005559.4:c.3081A>C MANE Select	NP_005550.2:p.Glu1027Asp