Canonical Allele Identifier: CA344236156

Gene: GPR37L1

Linked Data

• dbSNP Id: rs1306056701
• gnomAD v3: 1-202128425-T-C
• gnomAD v4: 1-202128425-T-C
• MyVariant Identifiers: chr1:g.202097553T>C (hg19) ; chr1:g.202128425T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128425T>C , CM000663.2:g.202128425T>C	GRCh38
NC_000001.10:g.202097553T>C , CM000663.1:g.202097553T>C	GRCh37
NC_000001.9:g.200364176T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.896T>C
ENST00000682545.1:c.*321T>C	ENSP00000508402.1:n.*321T>C
ENST00000682887.1:c.1716T>C	ENSP00000506946.1:n.1716T>C
ENST00000683302.1:c.1246T>C	ENSP00000507885.1:p.Cys416Arg
ENST00000683557.1:c.*147T>C	ENSP00000508029.1:n.*147T>C
ENST00000367282.6:c.1315T>C MANE Select	ENSP00000356251.4:p.Cys439Arg
ENST00000367282.5:c.1315T>C	ENSP00000356251.4:p.Cys439Arg
NM_004767.3:c.1315T>C	NP_004758.3:p.Cys439Arg
XM_011510158.1:c.754T>C	XP_011508460.1:p.Cys252Arg
NM_004767.4:c.1315T>C	NP_004758.3:p.Cys439Arg
XM_011510158.2:c.754T>C	XP_011508460.1:p.Cys252Arg
NM_004767.5:c.1315T>C MANE Select	NP_004758.3:p.Cys439Arg