Canonical Allele Identifier: CA355302216

Gene: CCDC39

Linked Data

• gnomAD v4: 3-180659529-G-T
• MyVariant Identifiers: chr3:g.180377317G>T (hg19) ; chr3:g.180659529G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659529G>T , CM000665.2:g.180659529G>T	GRCh38
NC_000003.11:g.180377317G>T , CM000665.1:g.180377317G>T	GRCh37
NC_000003.10:g.181860011G>T	NCBI36
NG_029581.1:g.24967C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.661C>A MANE Select	ENSP00000417960.2:p.Gln221Lys
ENST00000650641.1:n.740C>A
ENST00000650889.1:n.833C>A
ENST00000651046.1:c.661C>A	ENSP00000499175.1:p.Gln221Lys
ENST00000651818.1:n.803C>A
ENST00000652024.1:n.752C>A
ENST00000652408.1:n.798C>A
ENST00000442201.6:c.661C>A	ENSP00000405708.2:p.Gln221Lys
ENST00000476379.5:c.661C>A	ENSP00000417960.1:p.Gln221Lys
NM_181426.1:c.661C>A	NP_852091.1:p.Gln221Lys
NM_181426.2:c.661C>A MANE Select	NP_852091.1:p.Gln221Lys