Canonical Allele Identifier: CA401850659

Gene: LAMA1

Linked Data

• MyVariant Identifiers: chr18:g.7015841G>T (hg19) ; chr18:g.7015842G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.7015842G>T , CM000680.2:g.7015842G>T	GRCh38
NC_000018.9:g.7015841G>T , CM000680.1:g.7015841G>T	GRCh37
NC_000018.8:g.7005841G>T	NCBI36
NG_034251.1:g.106973C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389658.4:c.3006C>A MANE Select	ENSP00000374309.3:p.His1002Gln
ENST00000389658.3:c.3006C>A	ENSP00000374309.3:p.His1002Gln
ENST00000579014.5:n.4021C>A
NM_005559.3:c.3006C>A	NP_005550.2:p.His1002Gln
XM_011525655.1:c.3006C>A	XP_011523957.1:p.His1002Gln
XM_011525656.1:c.1434C>A	XP_011523958.1:p.His478Gln
XM_011525657.1:c.3006C>A	XP_011523959.1:p.His1002Gln
XM_011525655.2:c.3006C>A	XP_011523957.1:p.His1002Gln
XM_011525656.2:c.1434C>A	XP_011523958.1:p.His478Gln
NM_005559.4:c.3006C>A MANE Select	NP_005550.2:p.His1002Gln