Canonical Allele Identifier: CA1149139910

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128397_202128417delinsCTGCTGCTGCTGCTGCTGCTG , CM000663.2:g.202128397_202128417delinsCTGCTGCTGCTGCTGCTGCTG	GRCh38
NC_000001.10:g.202097525_202097545delinsCTGCTGCTGCTGCTGCTGCTG , CM000663.1:g.202097525_202097545delinsCTGCTGCTGCTGCTGCTGCTG	GRCh37
NC_000001.9:g.200364148_200364168delinsCTGCTGCTGCTGCTGCTGCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.868_888delinsCTGCTGCTGCTGCTGCTGCTG
ENST00000682545.1:c.*293_*313delinsCTGCTGCTGCTGCTGCTGCTG	ENSP00000508402.1:n.*293_*313delinsCTGCTGCTGCTGCTGCTGCTG
ENST00000682887.1:c.1688_1708delinsCTGCTGCTGCTGCTGCTGCTG	ENSP00000506946.1:n.1688_1708delinsCTGCTGCTGCTGCTGCTGCTG
ENST00000683302.1:c.1218_1238delinsCTGCTGCTGCTGCTGCTGCTG	ENSP00000507885.1:p.Asp406=
ENST00000683557.1:c.*119_*139delinsCTGCTGCTGCTGCTGCTGCTG	ENSP00000508029.1:n.*119_*139delinsCTGCTGCTGCTGCTGCTGCTG
ENST00000367282.6:c.1287_1307delinsCTGCTGCTGCTGCTGCTGCTG MANE Select	ENSP00000356251.4:p.Asp429=
ENST00000367282.5:c.1287_1307delinsCTGCTGCTGCTGCTGCTGCTG	ENSP00000356251.4:p.Asp429=
NM_004767.3:c.1287_1307delinsCTGCTGCTGCTGCTGCTGCTG	NP_004758.3:p.Asp429=
XM_011510158.1:c.726_746delinsCTGCTGCTGCTGCTGCTGCTG	XP_011508460.1:p.Asp242=
NM_004767.4:c.1287_1307delinsCTGCTGCTGCTGCTGCTGCTG	NP_004758.3:p.Asp429=
XM_011510158.2:c.726_746delinsCTGCTGCTGCTGCTGCTGCTG	XP_011508460.1:p.Asp242=
NM_004767.5:c.1287_1307delinsCTGCTGCTGCTGCTGCTGCTG MANE Select	NP_004758.3:p.Asp429=