Canonical Allele Identifier: CA344235932

Gene: GPR37L1

Linked Data

• COSMIC: COSM4135911
• MyVariant Identifiers: chr1:g.202097454T>G (hg19) ; chr1:g.202128326T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128326T>G , CM000663.2:g.202128326T>G	GRCh38
NC_000001.10:g.202097454T>G , CM000663.1:g.202097454T>G	GRCh37
NC_000001.9:g.200364077T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.797T>G
ENST00000682545.1:c.*222T>G	ENSP00000508402.1:n.*222T>G
ENST00000682887.1:c.1617T>G	ENSP00000506946.1:n.1617T>G
ENST00000683302.1:c.1147T>G	ENSP00000507885.1:p.Phe383Val
ENST00000683557.1:c.*48T>G	ENSP00000508029.1:n.*48T>G
ENST00000367282.6:c.1216T>G MANE Select	ENSP00000356251.4:p.Phe406Val
ENST00000367282.5:c.1216T>G	ENSP00000356251.4:p.Phe406Val
NM_004767.3:c.1216T>G	NP_004758.3:p.Phe406Val
XM_011510158.1:c.655T>G	XP_011508460.1:p.Phe219Val
NM_004767.4:c.1216T>G	NP_004758.3:p.Phe406Val
XM_011510158.2:c.655T>G	XP_011508460.1:p.Phe219Val
NM_004767.5:c.1216T>G MANE Select	NP_004758.3:p.Phe406Val