Canonical Allele Identifier: CA344236095

Gene: GPR37L1

Linked Data

• dbSNP Id: rs1300558792
• gnomAD v2: 1-202097531-C-A
• MyVariant Identifiers: chr1:g.202097531C>A (hg19) ; chr1:g.202128403C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128403C>A , CM000663.2:g.202128403C>A	GRCh38
NC_000001.10:g.202097531C>A , CM000663.1:g.202097531C>A	GRCh37
NC_000001.9:g.200364154C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.874C>A
ENST00000682545.1:c.*299C>A	ENSP00000508402.1:n.*299C>A
ENST00000682887.1:c.1694C>A	ENSP00000506946.1:n.1694C>A
ENST00000683302.1:c.1224C>A	ENSP00000507885.1:p.Cys408Ter
ENST00000683557.1:c.*125C>A	ENSP00000508029.1:n.*125C>A
ENST00000367282.6:c.1293C>A MANE Select	ENSP00000356251.4:p.Cys431Ter
ENST00000367282.5:c.1293C>A	ENSP00000356251.4:p.Cys431Ter
NM_004767.3:c.1293C>A	NP_004758.3:p.Cys431Ter
XM_011510158.1:c.732C>A	XP_011508460.1:p.Cys244Ter
NM_004767.4:c.1293C>A	NP_004758.3:p.Cys431Ter
XM_011510158.2:c.732C>A	XP_011508460.1:p.Cys244Ter
NM_004767.5:c.1293C>A MANE Select	NP_004758.3:p.Cys431Ter