Canonical Allele Identifier: CA2649858830

Gene: GPR37L1

Linked Data

• gnomAD v4: 1-202128276-TGACCCGCCA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128282_202128290del , CM000663.2:g.202128282_202128290del	GRCh38
NC_000001.10:g.202097410_202097418del , CM000663.1:g.202097410_202097418del	GRCh37
NC_000001.9:g.200364033_200364041del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.753_761del
ENST00000682545.1:c.*178_*186del	ENSP00000508402.1:n.*178_*186del
ENST00000682887.1:c.1573_1581del	ENSP00000506946.1:n.1573_1581del
ENST00000683302.1:c.1103_1111del	ENSP00000507885.1:p.Arg368_Thr370del
ENST00000683557.1:c.*4_*12del	ENSP00000508029.1:n.*4_*12del
ENST00000367282.6:c.1172_1180del MANE Select	ENSP00000356251.4:p.Arg391_Thr393del
ENST00000367282.5:c.1172_1180del	ENSP00000356251.4:p.Arg391_Thr393del
NM_004767.3:c.1172_1180del	NP_004758.3:p.Arg391_Thr393del
XM_011510158.1:c.611_619del	XP_011508460.1:p.Arg204_Thr206del
NM_004767.4:c.1172_1180del	NP_004758.3:p.Arg391_Thr393del
XM_011510158.2:c.611_619del	XP_011508460.1:p.Arg204_Thr206del
NM_004767.5:c.1172_1180del MANE Select	NP_004758.3:p.Arg391_Thr393del