Canonical Allele Identifier: CA422796263

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097384G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128256G>A , CM000663.2:g.202128256G>A	GRCh38
NC_000001.10:g.202097384G>A , CM000663.1:g.202097384G>A	GRCh37
NC_000001.9:g.200364007G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.727G>A
ENST00000682545.1:c.*152G>A	ENSP00000508402.1:n.*152G>A
ENST00000682887.1:c.1547G>A	ENSP00000506946.1:n.1547G>A
ENST00000683302.1:c.1077G>A	ENSP00000507885.1:p.Val359=
ENST00000683557.1:c.737G>A	ENSP00000508029.1:p.Trp246Ter
ENST00000367282.6:c.1146G>A MANE Select	ENSP00000356251.4:p.Val382=
ENST00000367282.5:c.1146G>A	ENSP00000356251.4:p.Val382=
NM_004767.3:c.1146G>A	NP_004758.3:p.Val382=
XM_011510158.1:c.585G>A	XP_011508460.1:p.Val195=
NM_004767.4:c.1146G>A	NP_004758.3:p.Val382=
XM_011510158.2:c.585G>A	XP_011508460.1:p.Val195=
NM_004767.5:c.1146G>A MANE Select	NP_004758.3:p.Val382=