Canonical Allele Identifier: CA401850540

Gene: LAMA1

Linked Data

• gnomAD v4: 18-7015787-G-C
• MyVariant Identifiers: chr18:g.7015786G>C (hg19) ; chr18:g.7015787G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.7015787G>C , CM000680.2:g.7015787G>C	GRCh38
NC_000018.9:g.7015786G>C , CM000680.1:g.7015786G>C	GRCh37
NC_000018.8:g.7005786G>C	NCBI36
NG_034251.1:g.107028C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389658.4:c.3061C>G MANE Select	ENSP00000374309.3:p.Gln1021Glu
ENST00000389658.3:c.3061C>G	ENSP00000374309.3:p.Gln1021Glu
ENST00000579014.5:n.4076C>G
NM_005559.3:c.3061C>G	NP_005550.2:p.Gln1021Glu
XM_011525655.1:c.3061C>G	XP_011523957.1:p.Gln1021Glu
XM_011525656.1:c.1489C>G	XP_011523958.1:p.Gln497Glu
XM_011525657.1:c.3061C>G	XP_011523959.1:p.Gln1021Glu
XM_011525655.2:c.3061C>G	XP_011523957.1:p.Gln1021Glu
XM_011525656.2:c.1489C>G	XP_011523958.1:p.Gln497Glu
NM_005559.4:c.3061C>G MANE Select	NP_005550.2:p.Gln1021Glu