Canonical Allele Identifier: CA1220026692

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128444_202128449delinsCCTCTG , CM000663.2:g.202128444_202128449delinsCCTCTG	GRCh38
NC_000001.10:g.202097572_202097577delinsCCTCTG , CM000663.1:g.202097572_202097577delinsCCTCTG	GRCh37
NC_000001.9:g.200364195_200364200delinsCCTCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.915_920delinsCCTCTG
ENST00000682545.1:c.*340_*345delinsCCTCTG	ENSP00000508402.1:n.*340_*345delinsCCTCTG
ENST00000682887.1:c.1735_1740delinsCCTCTG	ENSP00000506946.1:n.1735_1740delinsCCTCTG
ENST00000683302.1:c.1265_1270delinsCCTCTG	ENSP00000507885.1:p.Ala422=
ENST00000683557.1:c.*166_*171delinsCCTCTG	ENSP00000508029.1:n.*166_*171delinsCCTCTG
ENST00000367282.6:c.1334_1339delinsCCTCTG MANE Select	ENSP00000356251.4:p.Ala445=
ENST00000367282.5:c.1334_1339delinsCCTCTG	ENSP00000356251.4:p.Ala445=
NM_004767.3:c.1334_1339delinsCCTCTG	NP_004758.3:p.Ala445=
XM_011510158.1:c.773_778delinsCCTCTG	XP_011508460.1:p.Ala258=
NM_004767.4:c.1334_1339delinsCCTCTG	NP_004758.3:p.Ala445=
XM_011510158.2:c.773_778delinsCCTCTG	XP_011508460.1:p.Ala258=
NM_004767.5:c.1334_1339delinsCCTCTG MANE Select	NP_004758.3:p.Ala445=