Canonical Allele Identifier: CA987524443

Gene: LAMA1

Linked Data

• gnomAD v3: 18-7015588-G-GTTTTTTT
• gnomAD v4: 18-7015588-G-GTTTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.7015598_7015604dup , CM000680.2:g.7015598_7015604dup	GRCh38
NC_000018.9:g.7015597_7015603dup , CM000680.1:g.7015597_7015603dup	GRCh37
NC_000018.8:g.7005597_7005603dup	NCBI36
NG_034251.1:g.107220_107226dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389658.4:c.3126+127_3126+133dup MANE Select	ENSP00000374309.3:n.3126+127_3126+133dup
ENST00000389658.3:c.3126+127_3126+133dup	ENSP00000374309.3:n.3126+127_3126+133dup
ENST00000579014.5:n.4141+127_4141+133dup
NM_005559.3:c.3126+127_3126+133dup	NP_005550.2:n.3126+127_3126+133dup
XM_011525655.1:c.3126+127_3126+133dup	XP_011523957.1:n.3126+127_3126+133dup
XM_011525656.1:c.1554+127_1554+133dup	XP_011523958.1:n.1554+127_1554+133dup
XM_011525657.1:c.3126+127_3126+133dup	XP_011523959.1:n.3126+127_3126+133dup
XM_011525655.2:c.3126+127_3126+133dup	XP_011523957.1:n.3126+127_3126+133dup
XM_011525656.2:c.1554+127_1554+133dup	XP_011523958.1:n.1554+127_1554+133dup
NM_005559.4:c.3126+127_3126+133dup MANE Select	NP_005550.2:n.3126+127_3126+133dup