Canonical Allele Identifier: CA344235914

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097445T>G (hg19) ; chr1:g.202128317T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128317T>G , CM000663.2:g.202128317T>G	GRCh38
NC_000001.10:g.202097445T>G , CM000663.1:g.202097445T>G	GRCh37
NC_000001.9:g.200364068T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.788T>G
ENST00000682545.1:c.*213T>G	ENSP00000508402.1:n.*213T>G
ENST00000682887.1:c.1608T>G	ENSP00000506946.1:n.1608T>G
ENST00000683302.1:c.1138T>G	ENSP00000507885.1:p.Phe380Val
ENST00000683557.1:c.*39T>G	ENSP00000508029.1:n.*39T>G
ENST00000367282.6:c.1207T>G MANE Select	ENSP00000356251.4:p.Phe403Val
ENST00000367282.5:c.1207T>G	ENSP00000356251.4:p.Phe403Val
NM_004767.3:c.1207T>G	NP_004758.3:p.Phe403Val
XM_011510158.1:c.646T>G	XP_011508460.1:p.Phe216Val
NM_004767.4:c.1207T>G	NP_004758.3:p.Phe403Val
XM_011510158.2:c.646T>G	XP_011508460.1:p.Phe216Val
NM_004767.5:c.1207T>G MANE Select	NP_004758.3:p.Phe403Val