Canonical Allele Identifier: CA344236128

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097544T>C (hg19) ; chr1:g.202128416T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128416T>C , CM000663.2:g.202128416T>C	GRCh38
NC_000001.10:g.202097544T>C , CM000663.1:g.202097544T>C	GRCh37
NC_000001.9:g.200364167T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.887T>C
ENST00000682545.1:c.*312T>C	ENSP00000508402.1:n.*312T>C
ENST00000682887.1:c.1707T>C	ENSP00000506946.1:n.1707T>C
ENST00000683302.1:c.1237T>C	ENSP00000507885.1:p.Cys413Arg
ENST00000683557.1:c.*138T>C	ENSP00000508029.1:n.*138T>C
ENST00000367282.6:c.1306T>C MANE Select	ENSP00000356251.4:p.Cys436Arg
ENST00000367282.5:c.1306T>C	ENSP00000356251.4:p.Cys436Arg
NM_004767.3:c.1306T>C	NP_004758.3:p.Cys436Arg
XM_011510158.1:c.745T>C	XP_011508460.1:p.Cys249Arg
NM_004767.4:c.1306T>C	NP_004758.3:p.Cys436Arg
XM_011510158.2:c.745T>C	XP_011508460.1:p.Cys249Arg
NM_004767.5:c.1306T>C MANE Select	NP_004758.3:p.Cys436Arg