Canonical Allele Identifier: CA35471594

Gene: GPR37L1

Linked Data

• dbSNP Id: rs996890220
• gnomAD v3: 1-202128444-CCTCTG-C
• gnomAD v4: 1-202128444-CCTCTG-C
• MyVariant Identifiers: chr1:g.202097573_202097577del (hg19) ; chr1:g.202128445_202128449del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128447_202128451del , CM000663.2:g.202128447_202128451del	GRCh38
NC_000001.10:g.202097575_202097579del , CM000663.1:g.202097575_202097579del	GRCh37
NC_000001.9:g.200364198_200364202del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.918_922del
ENST00000682545.1:c.*343_*347del	ENSP00000508402.1:n.*343_*347del
ENST00000682887.1:c.1738_1742del	ENSP00000506946.1:n.1738_1742del
ENST00000683302.1:c.1268_1272del	ENSP00000507885.1:p.Ser423CysfsTer?
ENST00000683557.1:c.*169_*173del	ENSP00000508029.1:n.*169_*173del
ENST00000367282.6:c.1337_1341del MANE Select	ENSP00000356251.4:p.Ser446CysfsTer?
ENST00000367282.5:c.1337_1341del	ENSP00000356251.4:p.Ser446CysfsTer?
NM_004767.3:c.1337_1341del	NP_004758.3:p.Ser446CysfsTer?
XM_011510158.1:c.776_780del	XP_011508460.1:p.Ser259CysfsTer?
NM_004767.4:c.1337_1341del	NP_004758.3:p.Ser446CysfsTer?
XM_011510158.2:c.776_780del	XP_011508460.1:p.Ser259CysfsTer?
NM_004767.5:c.1337_1341del MANE Select	NP_004758.3:p.Ser446CysfsTer?