Canonical Allele Identifier: CA528528996

Gene: GPR37L1

Linked Data

• dbSNP Id: rs749733623
• gnomAD v2: 1-202097524-ACTGCTG-A
• gnomAD v4: 1-202128396-ACTGCTG-A
• MyVariant Identifiers: chr1:g.202097525_202097530del (hg19) ; chr1:g.202128397_202128402del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128412_202128417del , CM000663.2:g.202128412_202128417del	GRCh38
NC_000001.10:g.202097540_202097545del , CM000663.1:g.202097540_202097545del	GRCh37
NC_000001.9:g.200364163_200364168del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.883_888del
ENST00000682545.1:c.*308_*313del	ENSP00000508402.1:n.*308_*313del
ENST00000682887.1:c.1703_1708del	ENSP00000506946.1:n.1703_1708del
ENST00000683302.1:c.1233_1238del	ENSP00000507885.1:p.Cys412_Cys413del
ENST00000683557.1:c.*134_*139del	ENSP00000508029.1:n.*134_*139del
ENST00000367282.6:c.1302_1307del MANE Select	ENSP00000356251.4:p.Cys435_Cys436del
ENST00000367282.5:c.1302_1307del	ENSP00000356251.4:p.Cys435_Cys436del
NM_004767.3:c.1302_1307del	NP_004758.3:p.Cys435_Cys436del
XM_011510158.1:c.741_746del	XP_011508460.1:p.Cys248_Cys249del
NM_004767.4:c.1302_1307del	NP_004758.3:p.Cys435_Cys436del
XM_011510158.2:c.741_746del	XP_011508460.1:p.Cys248_Cys249del
NM_004767.5:c.1302_1307del MANE Select	NP_004758.3:p.Cys435_Cys436del