Canonical Allele Identifier: CA2282694512

Gene: LAMA1

Linked Data

• dbSNP Id: rs2057883276
• gnomAD v4: 18-7015571-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.7015571T>C , CM000680.2:g.7015571T>C	GRCh38
NC_000018.9:g.7015570T>C , CM000680.1:g.7015570T>C	GRCh37
NC_000018.8:g.7005570T>C	NCBI36
NG_034251.1:g.107244A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000389658.4:c.3126+151A>G MANE Select	ENSP00000374309.3:n.3126+151A>G
ENST00000389658.3:c.3126+151A>G	ENSP00000374309.3:n.3126+151A>G
ENST00000579014.5:n.4141+151A>G
NM_005559.3:c.3126+151A>G	NP_005550.2:n.3126+151A>G
XM_011525655.1:c.3126+151A>G	XP_011523957.1:n.3126+151A>G
XM_011525656.1:c.1554+151A>G	XP_011523958.1:n.1554+151A>G
XM_011525657.1:c.3126+151A>G	XP_011523959.1:n.3126+151A>G
XM_011525655.2:c.3126+151A>G	XP_011523957.1:n.3126+151A>G
XM_011525656.2:c.1554+151A>G	XP_011523958.1:n.1554+151A>G
NM_005559.4:c.3126+151A>G MANE Select	NP_005550.2:n.3126+151A>G