Canonical Allele Identifier: CA1220026688

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128434_202128435delinsGC , CM000663.2:g.202128434_202128435delinsGC	GRCh38
NC_000001.10:g.202097562_202097563delinsGC , CM000663.1:g.202097562_202097563delinsGC	GRCh37
NC_000001.9:g.200364185_200364186delinsGC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.905_906delinsGC
ENST00000682545.1:c.*330_*331delinsGC	ENSP00000508402.1:n.*330_*331delinsGC
ENST00000682887.1:c.1725_1726delinsGC	ENSP00000506946.1:n.1725_1726delinsGC
ENST00000683302.1:c.1255_1256delinsGC	ENSP00000507885.1:p.Ala419=
ENST00000683557.1:c.*156_*157delinsGC	ENSP00000508029.1:n.*156_*157delinsGC
ENST00000367282.6:c.1324_1325delinsGC MANE Select	ENSP00000356251.4:p.Ala442=
ENST00000367282.5:c.1324_1325delinsGC	ENSP00000356251.4:p.Ala442=
NM_004767.3:c.1324_1325delinsGC	NP_004758.3:p.Ala442=
XM_011510158.1:c.763_764delinsGC	XP_011508460.1:p.Ala255=
NM_004767.4:c.1324_1325delinsGC	NP_004758.3:p.Ala442=
XM_011510158.2:c.763_764delinsGC	XP_011508460.1:p.Ala255=
NM_004767.5:c.1324_1325delinsGC MANE Select	NP_004758.3:p.Ala442=