Canonical Allele Identifier: CA401850396

Gene: LAMA1

Linked Data

• dbSNP Id: rs1442325878
• gnomAD v2: 18-7015722-T-C
• gnomAD v4: 18-7015723-T-C
• MyVariant Identifiers: chr18:g.7015722T>C (hg19) ; chr18:g.7015723T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.7015723T>C , CM000680.2:g.7015723T>C	GRCh38
NC_000018.9:g.7015722T>C , CM000680.1:g.7015722T>C	GRCh37
NC_000018.8:g.7005722T>C	NCBI36
NG_034251.1:g.107092A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389658.4:c.3125A>G MANE Select	ENSP00000374309.3:p.Gln1042Arg
ENST00000389658.3:c.3125A>G	ENSP00000374309.3:p.Gln1042Arg
ENST00000579014.5:n.4140A>G
NM_005559.3:c.3125A>G	NP_005550.2:p.Gln1042Arg
XM_011525655.1:c.3125A>G	XP_011523957.1:p.Gln1042Arg
XM_011525656.1:c.1553A>G	XP_011523958.1:p.Gln518Arg
XM_011525657.1:c.3125A>G	XP_011523959.1:p.Gln1042Arg
XM_011525655.2:c.3125A>G	XP_011523957.1:p.Gln1042Arg
XM_011525656.2:c.1553A>G	XP_011523958.1:p.Gln518Arg
NM_005559.4:c.3125A>G MANE Select	NP_005550.2:p.Gln1042Arg