Canonical Allele Identifier: CA2606843296

Gene: GPR37L1

Linked Data

• dbSNP Id: rs2147806504
• gnomAD v3: 1-202128415-CTGT-C
• gnomAD v4: 1-202128415-CTGT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.202128416_202128418del , CM000663.2:g.202128416_202128418del	GRCh38
NC_000001.10:g.202097544_202097546del , CM000663.1:g.202097544_202097546del	GRCh37
NC_000001.9:g.200364167_200364169del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682422.1:n.887_889del
ENST00000682545.1:c.*312_*314del	ENSP00000508402.1:n.*312_*314del
ENST00000682887.1:c.1707_1709del	ENSP00000506946.1:n.1707_1709del
ENST00000683302.1:c.1237_1239del	ENSP00000507885.1:p.Cys413del
ENST00000683557.1:c.*138_*140del	ENSP00000508029.1:n.*138_*140del
ENST00000367282.6:c.1306_1308del MANE Select	ENSP00000356251.4:p.Cys436del
ENST00000367282.5:c.1306_1308del	ENSP00000356251.4:p.Cys436del
NM_004767.3:c.1306_1308del	NP_004758.3:p.Cys436del
XM_011510158.1:c.745_747del	XP_011508460.1:p.Cys249del
NM_004767.4:c.1306_1308del	NP_004758.3:p.Cys436del
XM_011510158.2:c.745_747del	XP_011508460.1:p.Cys249del
NM_004767.5:c.1306_1308del MANE Select	NP_004758.3:p.Cys436del