Canonical Allele Identifier: CA401850634

Gene: LAMA1

Linked Data

• MyVariant Identifiers: chr18:g.7015831T>A (hg19) ; chr18:g.7015832T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.7015832T>A , CM000680.2:g.7015832T>A	GRCh38
NC_000018.9:g.7015831T>A , CM000680.1:g.7015831T>A	GRCh37
NC_000018.8:g.7005831T>A	NCBI36
NG_034251.1:g.106983A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000389658.4:c.3016A>T MANE Select	ENSP00000374309.3:p.Thr1006Ser
ENST00000389658.3:c.3016A>T	ENSP00000374309.3:p.Thr1006Ser
ENST00000579014.5:n.4031A>T
NM_005559.3:c.3016A>T	NP_005550.2:p.Thr1006Ser
XM_011525655.1:c.3016A>T	XP_011523957.1:p.Thr1006Ser
XM_011525656.1:c.1444A>T	XP_011523958.1:p.Thr482Ser
XM_011525657.1:c.3016A>T	XP_011523959.1:p.Thr1006Ser
XM_011525655.2:c.3016A>T	XP_011523957.1:p.Thr1006Ser
XM_011525656.2:c.1444A>T	XP_011523958.1:p.Thr482Ser
NM_005559.4:c.3016A>T MANE Select	NP_005550.2:p.Thr1006Ser