Canonical Allele Identifier: CA344235827

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097401A>T (hg19) ; chr1:g.202128273A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128273A>T , CM000663.2:g.202128273A>T	GRCh38
NC_000001.10:g.202097401A>T , CM000663.1:g.202097401A>T	GRCh37
NC_000001.9:g.200364024A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.744A>T
ENST00000682545.1:c.*169A>T	ENSP00000508402.1:n.*169A>T
ENST00000682887.1:c.1564A>T	ENSP00000506946.1:n.1564A>T
ENST00000683302.1:c.1094A>T	ENSP00000507885.1:p.Glu365Val
ENST00000683557.1:c.754A>T	ENSP00000508029.1:p.Ser252Cys
ENST00000367282.6:c.1163A>T MANE Select	ENSP00000356251.4:p.Glu388Val
ENST00000367282.5:c.1163A>T	ENSP00000356251.4:p.Glu388Val
NM_004767.3:c.1163A>T	NP_004758.3:p.Glu388Val
XM_011510158.1:c.602A>T	XP_011508460.1:p.Glu201Val
NM_004767.4:c.1163A>T	NP_004758.3:p.Glu388Val
XM_011510158.2:c.602A>T	XP_011508460.1:p.Glu201Val
NM_004767.5:c.1163A>T MANE Select	NP_004758.3:p.Glu388Val