Canonical Allele Identifier: CA2282706927

Gene: LAMA1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.7042171T= , CM000680.2:g.7042171T=	GRCh38
NC_000018.9:g.7042170T= , CM000680.1:g.7042170T=	GRCh37
NC_000018.8:g.7032170T=	NCBI36
NG_034251.1:g.80644A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000389658.4:c.1235A= MANE Select	ENSP00000374309.3:p.Asp412=
ENST00000389658.3:c.1235A=	ENSP00000374309.3:p.Asp412=
ENST00000579014.5:n.2250A=
NM_005559.3:c.1235A=	NP_005550.2:p.Asp412=
XM_011525655.1:c.1235A=	XP_011523957.1:p.Asp412=
XM_011525657.1:c.1235A=	XP_011523959.1:p.Asp412=
XM_011525655.2:c.1235A=	XP_011523957.1:p.Asp412=
NM_005559.4:c.1235A= MANE Select	NP_005550.2:p.Asp412=