Canonical Allele Identifier: CA344236152

Gene: GPR37L1

Linked Data

• MyVariant Identifiers: chr1:g.202097551A>T (hg19) ; chr1:g.202128423A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128423A>T , CM000663.2:g.202128423A>T	GRCh38
NC_000001.10:g.202097551A>T , CM000663.1:g.202097551A>T	GRCh37
NC_000001.9:g.200364174A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.894A>T
ENST00000682545.1:c.*319A>T	ENSP00000508402.1:n.*319A>T
ENST00000682887.1:c.1714A>T	ENSP00000506946.1:n.1714A>T
ENST00000683302.1:c.1244A>T	ENSP00000507885.1:p.Glu415Val
ENST00000683557.1:c.*145A>T	ENSP00000508029.1:n.*145A>T
ENST00000367282.6:c.1313A>T MANE Select	ENSP00000356251.4:p.Glu438Val
ENST00000367282.5:c.1313A>T	ENSP00000356251.4:p.Glu438Val
NM_004767.3:c.1313A>T	NP_004758.3:p.Glu438Val
XM_011510158.1:c.752A>T	XP_011508460.1:p.Glu251Val
NM_004767.4:c.1313A>T	NP_004758.3:p.Glu438Val
XM_011510158.2:c.752A>T	XP_011508460.1:p.Glu251Val
NM_004767.5:c.1313A>T MANE Select	NP_004758.3:p.Glu438Val