Canonical Allele Identifier: CA422553950

Gene: GPR37L1

Linked Data

• dbSNP Id: rs1382443941
• gnomAD v2: 1-202097546-T-C
• gnomAD v4: 1-202128418-T-C
• MyVariant Identifiers: chr1:g.202097546T>C (hg19) ; chr1:g.202128418T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128418T>C , CM000663.2:g.202128418T>C	GRCh38
NC_000001.10:g.202097546T>C , CM000663.1:g.202097546T>C	GRCh37
NC_000001.9:g.200364169T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.889T>C
ENST00000682545.1:c.*314T>C	ENSP00000508402.1:n.*314T>C
ENST00000682887.1:c.1709T>C	ENSP00000506946.1:n.1709T>C
ENST00000683302.1:c.1239T>C	ENSP00000507885.1:p.Cys413=
ENST00000683557.1:c.*140T>C	ENSP00000508029.1:n.*140T>C
ENST00000367282.6:c.1308T>C MANE Select	ENSP00000356251.4:p.Cys436=
ENST00000367282.5:c.1308T>C	ENSP00000356251.4:p.Cys436=
NM_004767.3:c.1308T>C	NP_004758.3:p.Cys436=
XM_011510158.1:c.747T>C	XP_011508460.1:p.Cys249=
NM_004767.4:c.1308T>C	NP_004758.3:p.Cys436=
XM_011510158.2:c.747T>C	XP_011508460.1:p.Cys249=
NM_004767.5:c.1308T>C MANE Select	NP_004758.3:p.Cys436=