Canonical Allele Identifier: CA344236157

Gene: GPR37L1

Linked Data

• dbSNP Id: rs1306056701
• MyVariant Identifiers: chr1:g.202097553T>G (hg19) ; chr1:g.202128425T>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.896T>G
ENST00000682545.1:c.*321T>G	ENSP00000508402.1:n.*321T>G
ENST00000682887.1:c.1716T>G	ENSP00000506946.1:n.1716T>G
ENST00000683302.1:c.1246T>G	ENSP00000507885.1:p.Cys416Gly
ENST00000683557.1:c.*147T>G	ENSP00000508029.1:n.*147T>G
ENST00000367282.6:c.1315T>G MANE Select	ENSP00000356251.4:p.Cys439Gly
ENST00000367282.5:c.1315T>G	ENSP00000356251.4:p.Cys439Gly
NM_004767.3:c.1315T>G	NP_004758.3:p.Cys439Gly
XM_011510158.1:c.754T>G	XP_011508460.1:p.Cys252Gly
NM_004767.4:c.1315T>G	NP_004758.3:p.Cys439Gly
XM_011510158.2:c.754T>G	XP_011508460.1:p.Cys252Gly
NM_004767.5:c.1315T>G MANE Select	NP_004758.3:p.Cys439Gly