Canonical Allele Identifier: CA1330217

Gene: GPR37L1

Linked Data

• dbSNP Id: rs749733623
• ExAC: 1:202097524 A / ACTG
• gnomAD v2: 1-202097524-A-ACTG
• gnomAD v3: 1-202128396-A-ACTG
• gnomAD v4: 1-202128396-A-ACTG
• MyVariant Identifiers: chr1:g.202097530_202097531insCTG (hg19) ; chr1:g.202097527_202097528insCTG (hg19) ; chr1:g.202097524_202097525insCTG (hg19) ; chr1:g.202128402_202128403insCTG (hg38) ; chr1:g.202128399_202128400insCTG (hg38) ; chr1:g.202128396_202128397insCTG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128415_202128417dup , CM000663.2:g.202128415_202128417dup	GRCh38
NC_000001.10:g.202097543_202097545dup , CM000663.1:g.202097543_202097545dup	GRCh37
NC_000001.9:g.200364166_200364168dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.886_888dup
ENST00000682545.1:c.*311_*313dup	ENSP00000508402.1:n.*311_*313dup
ENST00000682887.1:c.1706_1708dup	ENSP00000506946.1:n.1706_1708dup
ENST00000683302.1:c.1236_1238dup	ENSP00000507885.1:p.Cys413_Glu414insCys
ENST00000683557.1:c.*137_*139dup	ENSP00000508029.1:n.*137_*139dup
ENST00000367282.6:c.1305_1307dup MANE Select	ENSP00000356251.4:p.Cys436_Glu437insCys
ENST00000367282.5:c.1305_1307dup	ENSP00000356251.4:p.Cys436_Glu437insCys
NM_004767.3:c.1305_1307dup	NP_004758.3:p.Cys436_Glu437insCys
XM_011510158.1:c.744_746dup	XP_011508460.1:p.Cys249_Glu250insCys
NM_004767.4:c.1305_1307dup	NP_004758.3:p.Cys436_Glu437insCys
XM_011510158.2:c.744_746dup	XP_011508460.1:p.Cys249_Glu250insCys
NM_004767.5:c.1305_1307dup MANE Select	NP_004758.3:p.Cys436_Glu437insCys