Canonical Allele Identifier: CA2282694434

Gene: LAMA1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.7015423_7015425delinsCCA , CM000680.2:g.7015423_7015425delinsCCA	GRCh38
NC_000018.9:g.7015422_7015424delinsCCA , CM000680.1:g.7015422_7015424delinsCCA	GRCh37
NC_000018.8:g.7005422_7005424delinsCCA	NCBI36
NG_034251.1:g.107390_107392delinsTGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389658.4:c.3126+297_3126+299delinsTGG MANE Select	ENSP00000374309.3:n.3126+297_3126+299delinsTGG
ENST00000389658.3:c.3126+297_3126+299delinsTGG	ENSP00000374309.3:n.3126+297_3126+299delinsTGG
ENST00000579014.5:n.4141+297_4141+299delinsTGG
NM_005559.3:c.3126+297_3126+299delinsTGG	NP_005550.2:n.3126+297_3126+299delinsTGG
XM_011525655.1:c.3126+297_3126+299delinsTGG	XP_011523957.1:n.3126+297_3126+299delinsTGG
XM_011525656.1:c.1554+297_1554+299delinsTGG	XP_011523958.1:n.1554+297_1554+299delinsTGG
XM_011525657.1:c.3126+297_3126+299delinsTGG	XP_011523959.1:n.3126+297_3126+299delinsTGG
XM_011525655.2:c.3126+297_3126+299delinsTGG	XP_011523957.1:n.3126+297_3126+299delinsTGG
XM_011525656.2:c.1554+297_1554+299delinsTGG	XP_011523958.1:n.1554+297_1554+299delinsTGG
NM_005559.4:c.3126+297_3126+299delinsTGG MANE Select	NP_005550.2:n.3126+297_3126+299delinsTGG