Canonical Allele Identifier: CA1330193

Gene: GPR37L1

Linked Data

• dbSNP Id: rs773384673
• ExAC: 1:202097410 G / A
• gnomAD v2: 1-202097410-G-A
• gnomAD v4: 1-202128282-G-A
• MyVariant Identifiers: chr1:g.202097410G>A (hg19) ; chr1:g.202128282G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128282G>A , CM000663.2:g.202128282G>A	GRCh38
NC_000001.10:g.202097410G>A , CM000663.1:g.202097410G>A	GRCh37
NC_000001.9:g.200364033G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.753G>A
ENST00000682545.1:c.*178G>A	ENSP00000508402.1:n.*178G>A
ENST00000682887.1:c.1573G>A	ENSP00000506946.1:n.1573G>A
ENST00000683302.1:c.1103G>A	ENSP00000507885.1:p.Arg368His
ENST00000683557.1:c.*4G>A	ENSP00000508029.1:n.*4G>A
ENST00000367282.6:c.1172G>A MANE Select	ENSP00000356251.4:p.Arg391His
ENST00000367282.5:c.1172G>A	ENSP00000356251.4:p.Arg391His
NM_004767.3:c.1172G>A	NP_004758.3:p.Arg391His
XM_011510158.1:c.611G>A	XP_011508460.1:p.Arg204His
NM_004767.4:c.1172G>A	NP_004758.3:p.Arg391His
XM_011510158.2:c.611G>A	XP_011508460.1:p.Arg204His
NM_004767.5:c.1172G>A MANE Select	NP_004758.3:p.Arg391His