Canonical Allele Identifier: CA2574111306

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128416_202128417insTCTGCTGCT , CM000663.2:g.202128416_202128417insTCTGCTGCT	GRCh38
NC_000001.10:g.202097544_202097545insTCTGCTGCT , CM000663.1:g.202097544_202097545insTCTGCTGCT	GRCh37
NC_000001.9:g.200364167_200364168insTCTGCTGCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.887_888insTCTGCTGCT
ENST00000682545.1:c.*312_*313insTCTGCTGCT	ENSP00000508402.1:n.*312_*313insTCTGCTGCT
ENST00000682887.1:c.1707_1708insTCTGCTGCT	ENSP00000506946.1:n.1707_1708insTCTGCTGCT
ENST00000683302.1:c.1237_1238insTCTGCTGCT	ENSP00000507885.1:p.Cys412_Cys413insPheCysCys
ENST00000683557.1:c.*138_*139insTCTGCTGCT	ENSP00000508029.1:n.*138_*139insTCTGCTGCT
ENST00000367282.6:c.1306_1307insTCTGCTGCT MANE Select	ENSP00000356251.4:p.Cys435_Cys436insPheCysCys
ENST00000367282.5:c.1306_1307insTCTGCTGCT	ENSP00000356251.4:p.Cys435_Cys436insPheCysCys
NM_004767.3:c.1306_1307insTCTGCTGCT	NP_004758.3:p.Cys435_Cys436insPheCysCys
XM_011510158.1:c.745_746insTCTGCTGCT	XP_011508460.1:p.Cys248_Cys249insPheCysCys
NM_004767.4:c.1306_1307insTCTGCTGCT	NP_004758.3:p.Cys435_Cys436insPheCysCys
XM_011510158.2:c.745_746insTCTGCTGCT	XP_011508460.1:p.Cys248_Cys249insPheCysCys
NM_004767.5:c.1306_1307insTCTGCTGCT MANE Select	NP_004758.3:p.Cys435_Cys436insPheCysCys