Canonical Allele Identifier: CA344236138

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097548A>T (hg19) ; chr1:g.202128420A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128420A>T , CM000663.2:g.202128420A>T	GRCh38
NC_000001.10:g.202097548A>T , CM000663.1:g.202097548A>T	GRCh37
NC_000001.9:g.200364171A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.891A>T
ENST00000682545.1:c.*316A>T	ENSP00000508402.1:n.*316A>T
ENST00000682887.1:c.1711A>T	ENSP00000506946.1:n.1711A>T
ENST00000683302.1:c.1241A>T	ENSP00000507885.1:p.Glu414Val
ENST00000683557.1:c.*142A>T	ENSP00000508029.1:n.*142A>T
ENST00000367282.6:c.1310A>T MANE Select	ENSP00000356251.4:p.Glu437Val
ENST00000367282.5:c.1310A>T	ENSP00000356251.4:p.Glu437Val
NM_004767.3:c.1310A>T	NP_004758.3:p.Glu437Val
XM_011510158.1:c.749A>T	XP_011508460.1:p.Glu250Val
NM_004767.4:c.1310A>T	NP_004758.3:p.Glu437Val
XM_011510158.2:c.749A>T	XP_011508460.1:p.Glu250Val
NM_004767.5:c.1310A>T MANE Select	NP_004758.3:p.Glu437Val