Canonical Allele Identifier: CA628132832

Gene: LAMA1

Linked Data

• dbSNP Id: rs1194513673
• gnomAD v2: 18-7015904-A-G
• gnomAD v3: 18-7015905-A-G
• gnomAD v4: 18-7015905-A-G
• MyVariant Identifiers: chr18:g.7015904A>G (hg19) ; chr18:g.7015905A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.7015905A>G , CM000680.2:g.7015905A>G	GRCh38
NC_000018.9:g.7015904A>G , CM000680.1:g.7015904A>G	GRCh37
NC_000018.8:g.7005904A>G	NCBI36
NG_034251.1:g.106910T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389658.4:c.2990-47T>C MANE Select	ENSP00000374309.3:n.2990-47T>C
ENST00000389658.3:c.2990-47T>C	ENSP00000374309.3:n.2990-47T>C
ENST00000579014.5:n.4005-47T>C
NM_005559.3:c.2990-47T>C	NP_005550.2:n.2990-47T>C
XM_011525655.1:c.2990-47T>C	XP_011523957.1:n.2990-47T>C
XM_011525656.1:c.1418-47T>C	XP_011523958.1:n.1418-47T>C
XM_011525657.1:c.2990-47T>C	XP_011523959.1:n.2990-47T>C
XM_011525655.2:c.2990-47T>C	XP_011523957.1:n.2990-47T>C
XM_011525656.2:c.1418-47T>C	XP_011523958.1:n.1418-47T>C
NM_005559.4:c.2990-47T>C MANE Select	NP_005550.2:n.2990-47T>C