Canonical Allele Identifier: CA422796193

Gene: GPR37L1

Linked Data

• dbSNP Id: rs200537062
• gnomAD v2: 1-202097318-C-A
• gnomAD v4: 1-202128190-C-A
• MyVariant Identifiers: chr1:g.202097318C>A (hg19) ; chr1:g.202128190C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128190C>A , CM000663.2:g.202128190C>A	GRCh38
NC_000001.10:g.202097318C>A , CM000663.1:g.202097318C>A	GRCh37
NC_000001.9:g.200363941C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.705-44C>A
ENST00000682545.1:c.*86C>A	ENSP00000508402.1:n.*86C>A
ENST00000682887.1:c.1481C>A	ENSP00000506946.1:n.1481C>A
ENST00000683302.1:c.1011C>A	ENSP00000507885.1:p.Thr337=
ENST00000683557.1:c.715-44C>A	ENSP00000508029.1:n.715-44C>A
ENST00000367282.6:c.1080C>A MANE Select	ENSP00000356251.4:p.Thr360=
ENST00000367282.5:c.1080C>A	ENSP00000356251.4:p.Thr360=
NM_004767.3:c.1080C>A	NP_004758.3:p.Thr360=
XM_011510158.1:c.519C>A	XP_011508460.1:p.Thr173=
NM_004767.4:c.1080C>A	NP_004758.3:p.Thr360=
XM_011510158.2:c.519C>A	XP_011508460.1:p.Thr173=
NM_004767.5:c.1080C>A MANE Select	NP_004758.3:p.Thr360=