Canonical Allele Identifier: CA8882401

Gene: LAMA1

Linked Data

• ClinVar Variation Id: 1421245
• ClinVar RCV Id: RCV001916826
• dbSNP Id: rs149260074
• ExAC: 18:7015737 G / A
• gnomAD v2: 18-7015737-G-A
• gnomAD v3: 18-7015738-G-A
• gnomAD v4: 18-7015738-G-A
• MyVariant Identifiers: chr18:g.7015737G>A (hg19) ; chr18:g.7015738G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.7015738G>A , CM000680.2:g.7015738G>A	GRCh38
NC_000018.9:g.7015737G>A , CM000680.1:g.7015737G>A	GRCh37
NC_000018.8:g.7005737G>A	NCBI36
NG_034251.1:g.107077C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000389658.4:c.3110C>T MANE Select	ENSP00000374309.3:p.Ala1037Val
ENST00000389658.3:c.3110C>T	ENSP00000374309.3:p.Ala1037Val
ENST00000579014.5:n.4125C>T
NM_005559.3:c.3110C>T	NP_005550.2:p.Ala1037Val
XM_011525655.1:c.3110C>T	XP_011523957.1:p.Ala1037Val
XM_011525656.1:c.1538C>T	XP_011523958.1:p.Ala513Val
XM_011525657.1:c.3110C>T	XP_011523959.1:p.Ala1037Val
XM_011525655.2:c.3110C>T	XP_011523957.1:p.Ala1037Val
XM_011525656.2:c.1538C>T	XP_011523958.1:p.Ala513Val
NM_005559.4:c.3110C>T MANE Select	NP_005550.2:p.Ala1037Val