Canonical Allele Identifier: CA2282694500

Gene: LAMA1

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.7015559_7015560delinsTG , CM000680.2:g.7015559_7015560delinsTG	GRCh38
NC_000018.9:g.7015558_7015559delinsTG , CM000680.1:g.7015558_7015559delinsTG	GRCh37
NC_000018.8:g.7005558_7005559delinsTG	NCBI36
NG_034251.1:g.107255_107256delinsCA

Transcript Alleles

HGVS	Amino-acid change
ENST00000389658.4:c.3126+162_3126+163delinsCA MANE Select	ENSP00000374309.3:n.3126+162_3126+163delinsCA
ENST00000389658.3:c.3126+162_3126+163delinsCA	ENSP00000374309.3:n.3126+162_3126+163delinsCA
ENST00000579014.5:n.4141+162_4141+163delinsCA
NM_005559.3:c.3126+162_3126+163delinsCA	NP_005550.2:n.3126+162_3126+163delinsCA
XM_011525655.1:c.3126+162_3126+163delinsCA	XP_011523957.1:n.3126+162_3126+163delinsCA
XM_011525656.1:c.1554+162_1554+163delinsCA	XP_011523958.1:n.1554+162_1554+163delinsCA
XM_011525657.1:c.3126+162_3126+163delinsCA	XP_011523959.1:n.3126+162_3126+163delinsCA
XM_011525655.2:c.3126+162_3126+163delinsCA	XP_011523957.1:n.3126+162_3126+163delinsCA
XM_011525656.2:c.1554+162_1554+163delinsCA	XP_011523958.1:n.1554+162_1554+163delinsCA
NM_005559.4:c.3126+162_3126+163delinsCA MANE Select	NP_005550.2:n.3126+162_3126+163delinsCA