Canonical Allele Identifier: CA2282694484

Gene: LAMA1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.7015519_7015522delinsATCC , CM000680.2:g.7015519_7015522delinsATCC	GRCh38
NC_000018.9:g.7015518_7015521delinsATCC , CM000680.1:g.7015518_7015521delinsATCC	GRCh37
NC_000018.8:g.7005518_7005521delinsATCC	NCBI36
NG_034251.1:g.107293_107296delinsGGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389658.4:c.3126+200_3126+203delinsGGAT MANE Select	ENSP00000374309.3:n.3126+200_3126+203delinsGGAT
ENST00000389658.3:c.3126+200_3126+203delinsGGAT	ENSP00000374309.3:n.3126+200_3126+203delinsGGAT
ENST00000579014.5:n.4141+200_4141+203delinsGGAT
NM_005559.3:c.3126+200_3126+203delinsGGAT	NP_005550.2:n.3126+200_3126+203delinsGGAT
XM_011525655.1:c.3126+200_3126+203delinsGGAT	XP_011523957.1:n.3126+200_3126+203delinsGGAT
XM_011525656.1:c.1554+200_1554+203delinsGGAT	XP_011523958.1:n.1554+200_1554+203delinsGGAT
XM_011525657.1:c.3126+200_3126+203delinsGGAT	XP_011523959.1:n.3126+200_3126+203delinsGGAT
XM_011525655.2:c.3126+200_3126+203delinsGGAT	XP_011523957.1:n.3126+200_3126+203delinsGGAT
XM_011525656.2:c.1554+200_1554+203delinsGGAT	XP_011523958.1:n.1554+200_1554+203delinsGGAT
NM_005559.4:c.3126+200_3126+203delinsGGAT MANE Select	NP_005550.2:n.3126+200_3126+203delinsGGAT