Canonical Allele Identifier: CA781976214

Gene: LAMA1

Linked Data

• dbSNP Id: rs1177610546
• gnomAD v3: 18-7015437-AT-A
• gnomAD v4: 18-7015437-AT-A
• MyVariant Identifiers: chr18:g.7015437del (hg19) ; chr18:g.7015438del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.7015446del , CM000680.2:g.7015446del	GRCh38
NC_000018.9:g.7015445del , CM000680.1:g.7015445del	GRCh37
NC_000018.8:g.7005445del	NCBI36
NG_034251.1:g.107377del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389658.4:c.3126+284del MANE Select	ENSP00000374309.3:n.3126+284del
ENST00000389658.3:c.3126+284del	ENSP00000374309.3:n.3126+284del
ENST00000579014.5:n.4141+284del
NM_005559.3:c.3126+284del	NP_005550.2:n.3126+284del
XM_011525655.1:c.3126+284del	XP_011523957.1:n.3126+284del
XM_011525656.1:c.1554+284del	XP_011523958.1:n.1554+284del
XM_011525657.1:c.3126+284del	XP_011523959.1:n.3126+284del
XM_011525655.2:c.3126+284del	XP_011523957.1:n.3126+284del
XM_011525656.2:c.1554+284del	XP_011523958.1:n.1554+284del
NM_005559.4:c.3126+284del MANE Select	NP_005550.2:n.3126+284del