Canonical Allele Identifier: CA1220026674

Gene: GPR37L1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128396_202128402delinsACTGCTG , CM000663.2:g.202128396_202128402delinsACTGCTG	GRCh38
NC_000001.10:g.202097524_202097530delinsACTGCTG , CM000663.1:g.202097524_202097530delinsACTGCTG	GRCh37
NC_000001.9:g.200364147_200364153delinsACTGCTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.867_873delinsACTGCTG
ENST00000682545.1:c.*292_*298delinsACTGCTG	ENSP00000508402.1:n.*292_*298delinsACTGCTG
ENST00000682887.1:c.1687_1693delinsACTGCTG	ENSP00000506946.1:n.1687_1693delinsACTGCTG
ENST00000683302.1:c.1217_1223delinsACTGCTG	ENSP00000507885.1:p.Asp406=
ENST00000683557.1:c.*118_*124delinsACTGCTG	ENSP00000508029.1:n.*118_*124delinsACTGCTG
ENST00000367282.6:c.1286_1292delinsACTGCTG MANE Select	ENSP00000356251.4:p.Asp429=
ENST00000367282.5:c.1286_1292delinsACTGCTG	ENSP00000356251.4:p.Asp429=
NM_004767.3:c.1286_1292delinsACTGCTG	NP_004758.3:p.Asp429=
XM_011510158.1:c.725_731delinsACTGCTG	XP_011508460.1:p.Asp242=
NM_004767.4:c.1286_1292delinsACTGCTG	NP_004758.3:p.Asp429=
XM_011510158.2:c.725_731delinsACTGCTG	XP_011508460.1:p.Asp242=
NM_004767.5:c.1286_1292delinsACTGCTG MANE Select	NP_004758.3:p.Asp429=