Canonical Allele Identifier: CA2282694447

Gene: LAMA1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.7015437_7015438delinsAT , CM000680.2:g.7015437_7015438delinsAT	GRCh38
NC_000018.9:g.7015436_7015437delinsAT , CM000680.1:g.7015436_7015437delinsAT	GRCh37
NC_000018.8:g.7005436_7005437delinsAT	NCBI36
NG_034251.1:g.107377_107378delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389658.4:c.3126+284_3126+285delinsAT MANE Select	ENSP00000374309.3:n.3126+284_3126+285delinsAT
ENST00000389658.3:c.3126+284_3126+285delinsAT	ENSP00000374309.3:n.3126+284_3126+285delinsAT
ENST00000579014.5:n.4141+284_4141+285delinsAT
NM_005559.3:c.3126+284_3126+285delinsAT	NP_005550.2:n.3126+284_3126+285delinsAT
XM_011525655.1:c.3126+284_3126+285delinsAT	XP_011523957.1:n.3126+284_3126+285delinsAT
XM_011525656.1:c.1554+284_1554+285delinsAT	XP_011523958.1:n.1554+284_1554+285delinsAT
XM_011525657.1:c.3126+284_3126+285delinsAT	XP_011523959.1:n.3126+284_3126+285delinsAT
XM_011525655.2:c.3126+284_3126+285delinsAT	XP_011523957.1:n.3126+284_3126+285delinsAT
XM_011525656.2:c.1554+284_1554+285delinsAT	XP_011523958.1:n.1554+284_1554+285delinsAT
NM_005559.4:c.3126+284_3126+285delinsAT MANE Select	NP_005550.2:n.3126+284_3126+285delinsAT