Canonical Allele Identifier: CA2640920078

Gene: LAMA1

Linked Data

• gnomAD v4: 18-7015587-A-ATT

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.7015587_7015588insTT , CM000680.2:g.7015587_7015588insTT	GRCh38
NC_000018.9:g.7015586_7015587insTT , CM000680.1:g.7015586_7015587insTT	GRCh37
NC_000018.8:g.7005586_7005587insTT	NCBI36
NG_034251.1:g.107227_107228insAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389658.4:c.3126+134_3126+135insAA MANE Select	ENSP00000374309.3:n.3126+134_3126+135insAA
ENST00000389658.3:c.3126+134_3126+135insAA	ENSP00000374309.3:n.3126+134_3126+135insAA
ENST00000579014.5:n.4141+134_4141+135insAA
NM_005559.3:c.3126+134_3126+135insAA	NP_005550.2:n.3126+134_3126+135insAA
XM_011525655.1:c.3126+134_3126+135insAA	XP_011523957.1:n.3126+134_3126+135insAA
XM_011525656.1:c.1554+134_1554+135insAA	XP_011523958.1:n.1554+134_1554+135insAA
XM_011525657.1:c.3126+134_3126+135insAA	XP_011523959.1:n.3126+134_3126+135insAA
XM_011525655.2:c.3126+134_3126+135insAA	XP_011523957.1:n.3126+134_3126+135insAA
XM_011525656.2:c.1554+134_1554+135insAA	XP_011523958.1:n.1554+134_1554+135insAA
NM_005559.4:c.3126+134_3126+135insAA MANE Select	NP_005550.2:n.3126+134_3126+135insAA