Canonical Allele Identifier: CA344236155

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097553T>A (hg19) ; chr1:g.202128425T>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.896T>A
ENST00000682545.1:c.*321T>A	ENSP00000508402.1:n.*321T>A
ENST00000682887.1:c.1716T>A	ENSP00000506946.1:n.1716T>A
ENST00000683302.1:c.1246T>A	ENSP00000507885.1:p.Cys416Ser
ENST00000683557.1:c.*147T>A	ENSP00000508029.1:n.*147T>A
ENST00000367282.6:c.1315T>A MANE Select	ENSP00000356251.4:p.Cys439Ser
ENST00000367282.5:c.1315T>A	ENSP00000356251.4:p.Cys439Ser
NM_004767.3:c.1315T>A	NP_004758.3:p.Cys439Ser
XM_011510158.1:c.754T>A	XP_011508460.1:p.Cys252Ser
NM_004767.4:c.1315T>A	NP_004758.3:p.Cys439Ser
XM_011510158.2:c.754T>A	XP_011508460.1:p.Cys252Ser
NM_004767.5:c.1315T>A MANE Select	NP_004758.3:p.Cys439Ser