Canonical Allele Identifier: CA548337193

Gene: CCDC39

Linked Data

• dbSNP Id: rs1323140278
• gnomAD v2: 3-180377410-G-T
• gnomAD v4: 3-180659622-G-T
• MyVariant Identifiers: chr3:g.180377410G>T (hg19) ; chr3:g.180659622G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659622G>T , CM000665.2:g.180659622G>T	GRCh38
NC_000003.11:g.180377410G>T , CM000665.1:g.180377410G>T	GRCh37
NC_000003.10:g.181860104G>T	NCBI36
NG_029581.1:g.24874C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.610-42C>A MANE Select	ENSP00000417960.2:n.610-42C>A
ENST00000650641.1:n.689-42C>A
ENST00000650889.1:n.782-42C>A
ENST00000651046.1:c.610-42C>A	ENSP00000499175.1:n.610-42C>A
ENST00000651818.1:n.752-42C>A
ENST00000652024.1:n.701-42C>A
ENST00000652408.1:n.747-42C>A
ENST00000442201.6:c.610-42C>A	ENSP00000405708.2:n.610-42C>A
ENST00000476379.5:c.610-42C>A	ENSP00000417960.1:n.610-42C>A
NM_181426.1:c.610-42C>A	NP_852091.1:n.610-42C>A
NM_181426.2:c.610-42C>A MANE Select	NP_852091.1:n.610-42C>A