Canonical Allele Identifier: CA2282694582

Gene: LAMA1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.7015702G= , CM000680.2:g.7015702G=	GRCh38
NC_000018.9:g.7015701G= , CM000680.1:g.7015701G=	GRCh37
NC_000018.8:g.7005701G=	NCBI36
NG_034251.1:g.107113C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389658.4:c.3126+20C= MANE Select	ENSP00000374309.3:n.3126+20C=
ENST00000389658.3:c.3126+20C=	ENSP00000374309.3:n.3126+20C=
ENST00000579014.5:n.4141+20C=
NM_005559.3:c.3126+20C=	NP_005550.2:n.3126+20C=
XM_011525655.1:c.3126+20C=	XP_011523957.1:n.3126+20C=
XM_011525656.1:c.1554+20C=	XP_011523958.1:n.1554+20C=
XM_011525657.1:c.3126+20C=	XP_011523959.1:n.3126+20C=
XM_011525655.2:c.3126+20C=	XP_011523957.1:n.3126+20C=
XM_011525656.2:c.1554+20C=	XP_011523958.1:n.1554+20C=
NM_005559.4:c.3126+20C= MANE Select	NP_005550.2:n.3126+20C=