Canonical Allele Identifier: CA344235615

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097300G>T (hg19) ; chr1:g.202128172G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128172G>T , CM000663.2:g.202128172G>T	GRCh38
NC_000001.10:g.202097300G>T , CM000663.1:g.202097300G>T	GRCh37
NC_000001.9:g.200363923G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.705-62G>T
ENST00000682545.1:c.*68G>T	ENSP00000508402.1:n.*68G>T
ENST00000682887.1:c.1463G>T	ENSP00000506946.1:n.1463G>T
ENST00000683302.1:c.993G>T	ENSP00000507885.1:p.Glu331Asp
ENST00000683557.1:c.715-62G>T	ENSP00000508029.1:n.715-62G>T
ENST00000367282.6:c.1062G>T MANE Select	ENSP00000356251.4:p.Glu354Asp
ENST00000367282.5:c.1062G>T	ENSP00000356251.4:p.Glu354Asp
NM_004767.3:c.1062G>T	NP_004758.3:p.Glu354Asp
XM_011510158.1:c.501G>T	XP_011508460.1:p.Glu167Asp
NM_004767.4:c.1062G>T	NP_004758.3:p.Glu354Asp
XM_011510158.2:c.501G>T	XP_011508460.1:p.Glu167Asp
NM_004767.5:c.1062G>T MANE Select	NP_004758.3:p.Glu354Asp