Canonical Allele Identifier: CA344236089

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097529T>A (hg19) ; chr1:g.202128401T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128401T>A , CM000663.2:g.202128401T>A	GRCh38
NC_000001.10:g.202097529T>A , CM000663.1:g.202097529T>A	GRCh37
NC_000001.9:g.200364152T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.872T>A
ENST00000682545.1:c.*297T>A	ENSP00000508402.1:n.*297T>A
ENST00000682887.1:c.1692T>A	ENSP00000506946.1:n.1692T>A
ENST00000683302.1:c.1222T>A	ENSP00000507885.1:p.Cys408Ser
ENST00000683557.1:c.*123T>A	ENSP00000508029.1:n.*123T>A
ENST00000367282.6:c.1291T>A MANE Select	ENSP00000356251.4:p.Cys431Ser
ENST00000367282.5:c.1291T>A	ENSP00000356251.4:p.Cys431Ser
NM_004767.3:c.1291T>A	NP_004758.3:p.Cys431Ser
XM_011510158.1:c.730T>A	XP_011508460.1:p.Cys244Ser
NM_004767.4:c.1291T>A	NP_004758.3:p.Cys431Ser
XM_011510158.2:c.730T>A	XP_011508460.1:p.Cys244Ser
NM_004767.5:c.1291T>A MANE Select	NP_004758.3:p.Cys431Ser