Canonical Allele Identifier: CA344236129

Gene: GPR37L1

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.887T>G
ENST00000682545.1:c.*312T>G	ENSP00000508402.1:n.*312T>G
ENST00000682887.1:c.1707T>G	ENSP00000506946.1:n.1707T>G
ENST00000683302.1:c.1237T>G	ENSP00000507885.1:p.Cys413Gly
ENST00000683557.1:c.*138T>G	ENSP00000508029.1:n.*138T>G
ENST00000367282.6:c.1306T>G MANE Select	ENSP00000356251.4:p.Cys436Gly
ENST00000367282.5:c.1306T>G	ENSP00000356251.4:p.Cys436Gly
NM_004767.3:c.1306T>G	NP_004758.3:p.Cys436Gly
XM_011510158.1:c.745T>G	XP_011508460.1:p.Cys249Gly
NM_004767.4:c.1306T>G	NP_004758.3:p.Cys436Gly
XM_011510158.2:c.745T>G	XP_011508460.1:p.Cys249Gly
NM_004767.5:c.1306T>G MANE Select	NP_004758.3:p.Cys436Gly