Canonical Allele Identifier: CA1424310434

Gene: CCDC39

Linked Data

• dbSNP Id: rs1711690763
• gnomAD v4: 3-180659629-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659629C>A , CM000665.2:g.180659629C>A	GRCh38
NC_000003.11:g.180377417C>A , CM000665.1:g.180377417C>A	GRCh37
NC_000003.10:g.181860111C>A	NCBI36
NG_029581.1:g.24867G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.610-49G>T MANE Select	ENSP00000417960.2:n.610-49G>T
ENST00000650641.1:n.689-49G>T
ENST00000650889.1:n.782-49G>T
ENST00000651046.1:c.610-49G>T	ENSP00000499175.1:n.610-49G>T
ENST00000651818.1:n.752-49G>T
ENST00000652024.1:n.701-49G>T
ENST00000652408.1:n.747-49G>T
ENST00000442201.6:c.610-49G>T	ENSP00000405708.2:n.610-49G>T
ENST00000476379.5:c.610-49G>T	ENSP00000417960.1:n.610-49G>T
NM_181426.1:c.610-49G>T	NP_852091.1:n.610-49G>T
NM_181426.2:c.610-49G>T MANE Select	NP_852091.1:n.610-49G>T