Canonical Allele Identifier: CA2734588293

Gene: LAMA1

Linked Data

• dbSNP Id: rs2144184179

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.7042066A>G , CM000680.2:g.7042066A>G	GRCh38
NC_000018.9:g.7042065A>G , CM000680.1:g.7042065A>G	GRCh37
NC_000018.8:g.7032065A>G	NCBI36
NG_034251.1:g.80749T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000389658.4:c.1261+79T>C MANE Select	ENSP00000374309.3:n.1261+79T>C
ENST00000389658.3:c.1261+79T>C	ENSP00000374309.3:n.1261+79T>C
ENST00000579014.5:n.2276+79T>C
NM_005559.3:c.1261+79T>C	NP_005550.2:n.1261+79T>C
XM_011525655.1:c.1261+79T>C	XP_011523957.1:n.1261+79T>C
XM_011525657.1:c.1261+79T>C	XP_011523959.1:n.1261+79T>C
XM_011525655.2:c.1261+79T>C	XP_011523957.1:n.1261+79T>C
NM_005559.4:c.1261+79T>C MANE Select	NP_005550.2:n.1261+79T>C