Canonical Allele Identifier: CA344236188

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097569A>T (hg19) ; chr1:g.202128441A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128441A>T , CM000663.2:g.202128441A>T	GRCh38
NC_000001.10:g.202097569A>T , CM000663.1:g.202097569A>T	GRCh37
NC_000001.9:g.200364192A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.912A>T
ENST00000682545.1:c.*337A>T	ENSP00000508402.1:n.*337A>T
ENST00000682887.1:c.1732A>T	ENSP00000506946.1:n.1732A>T
ENST00000683302.1:c.1262A>T	ENSP00000507885.1:p.Glu421Val
ENST00000683557.1:c.*163A>T	ENSP00000508029.1:n.*163A>T
ENST00000367282.6:c.1331A>T MANE Select	ENSP00000356251.4:p.Glu444Val
ENST00000367282.5:c.1331A>T	ENSP00000356251.4:p.Glu444Val
NM_004767.3:c.1331A>T	NP_004758.3:p.Glu444Val
XM_011510158.1:c.770A>T	XP_011508460.1:p.Glu257Val
NM_004767.4:c.1331A>T	NP_004758.3:p.Glu444Val
XM_011510158.2:c.770A>T	XP_011508460.1:p.Glu257Val
NM_004767.5:c.1331A>T MANE Select	NP_004758.3:p.Glu444Val