Canonical Allele Identifier: CA2530810396

Gene: CCDC39

Linked Data

• gnomAD v4: 3-180659603-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659603C>T , CM000665.2:g.180659603C>T	GRCh38
NC_000003.11:g.180377391C>T , CM000665.1:g.180377391C>T	GRCh37
NC_000003.10:g.181860085C>T	NCBI36
NG_029581.1:g.24893G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.610-23G>A MANE Select	ENSP00000417960.2:n.610-23G>A
ENST00000650641.1:n.689-23G>A
ENST00000650889.1:n.782-23G>A
ENST00000651046.1:c.610-23G>A	ENSP00000499175.1:n.610-23G>A
ENST00000651818.1:n.752-23G>A
ENST00000652024.1:n.701-23G>A
ENST00000652408.1:n.747-23G>A
ENST00000442201.6:c.610-23G>A	ENSP00000405708.2:n.610-23G>A
ENST00000476379.5:c.610-23G>A	ENSP00000417960.1:n.610-23G>A
NM_181426.1:c.610-23G>A	NP_852091.1:n.610-23G>A
NM_181426.2:c.610-23G>A MANE Select	NP_852091.1:n.610-23G>A