Canonical Allele Identifier: CA422796400

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097468C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128340C>A , CM000663.2:g.202128340C>A	GRCh38
NC_000001.10:g.202097468C>A , CM000663.1:g.202097468C>A	GRCh37
NC_000001.9:g.200364091C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.811C>A
ENST00000682545.1:c.*236C>A	ENSP00000508402.1:n.*236C>A
ENST00000682887.1:c.1631C>A	ENSP00000506946.1:n.1631C>A
ENST00000683302.1:c.1161C>A	ENSP00000507885.1:p.Ala387=
ENST00000683557.1:c.*62C>A	ENSP00000508029.1:n.*62C>A
ENST00000367282.6:c.1230C>A MANE Select	ENSP00000356251.4:p.Ala410=
ENST00000367282.5:c.1230C>A	ENSP00000356251.4:p.Ala410=
NM_004767.3:c.1230C>A	NP_004758.3:p.Ala410=
XM_011510158.1:c.669C>A	XP_011508460.1:p.Ala223=
NM_004767.4:c.1230C>A	NP_004758.3:p.Ala410=
XM_011510158.2:c.669C>A	XP_011508460.1:p.Ala223=
NM_004767.5:c.1230C>A MANE Select	NP_004758.3:p.Ala410=