Canonical Allele Identifier: CA2640920163

Gene: LAMA1

Linked Data

• gnomAD v4: 18-7015695-AGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.7015696_7015697del , CM000680.2:g.7015696_7015697del	GRCh38
NC_000018.9:g.7015695_7015696del , CM000680.1:g.7015695_7015696del	GRCh37
NC_000018.8:g.7005695_7005696del	NCBI36
NG_034251.1:g.107118_107119del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389658.4:c.3126+25_3126+26del MANE Select	ENSP00000374309.3:n.3126+25_3126+26del
ENST00000389658.3:c.3126+25_3126+26del	ENSP00000374309.3:n.3126+25_3126+26del
ENST00000579014.5:n.4141+25_4141+26del
NM_005559.3:c.3126+25_3126+26del	NP_005550.2:n.3126+25_3126+26del
XM_011525655.1:c.3126+25_3126+26del	XP_011523957.1:n.3126+25_3126+26del
XM_011525656.1:c.1554+25_1554+26del	XP_011523958.1:n.1554+25_1554+26del
XM_011525657.1:c.3126+25_3126+26del	XP_011523959.1:n.3126+25_3126+26del
XM_011525655.2:c.3126+25_3126+26del	XP_011523957.1:n.3126+25_3126+26del
XM_011525656.2:c.1554+25_1554+26del	XP_011523958.1:n.1554+25_1554+26del
NM_005559.4:c.3126+25_3126+26del MANE Select	NP_005550.2:n.3126+25_3126+26del