Canonical Allele Identifier: CA401850422

Gene: LAMA1

Linked Data

• dbSNP Id: rs1600395086
• MyVariant Identifiers: chr18:g.7015734T>C (hg19) ; chr18:g.7015735T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.7015735T>C , CM000680.2:g.7015735T>C	GRCh38
NC_000018.9:g.7015734T>C , CM000680.1:g.7015734T>C	GRCh37
NC_000018.8:g.7005734T>C	NCBI36
NG_034251.1:g.107080A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000389658.4:c.3113A>G MANE Select	ENSP00000374309.3:p.Glu1038Gly
ENST00000389658.3:c.3113A>G	ENSP00000374309.3:p.Glu1038Gly
ENST00000579014.5:n.4128A>G
NM_005559.3:c.3113A>G	NP_005550.2:p.Glu1038Gly
XM_011525655.1:c.3113A>G	XP_011523957.1:p.Glu1038Gly
XM_011525656.1:c.1541A>G	XP_011523958.1:p.Glu514Gly
XM_011525657.1:c.3113A>G	XP_011523959.1:p.Glu1038Gly
XM_011525655.2:c.3113A>G	XP_011523957.1:p.Glu1038Gly
XM_011525656.2:c.1541A>G	XP_011523958.1:p.Glu514Gly
NM_005559.4:c.3113A>G MANE Select	NP_005550.2:p.Glu1038Gly