Canonical Allele Identifier: CA1424310438

Gene: CCDC39

Linked Data

• dbSNP Id: rs746761136

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180659638C>A , CM000665.2:g.180659638C>A	GRCh38
NC_000003.11:g.180377426C>A , CM000665.1:g.180377426C>A	GRCh37
NC_000003.10:g.181860120C>A	NCBI36
NG_029581.1:g.24858G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.609+39G>T MANE Select	ENSP00000417960.2:n.609+39G>T
ENST00000650641.1:n.688+39G>T
ENST00000650889.1:n.781+39G>T
ENST00000651046.1:c.609+39G>T	ENSP00000499175.1:n.609+39G>T
ENST00000651818.1:n.751+39G>T
ENST00000652024.1:n.700+39G>T
ENST00000652408.1:n.746+39G>T
ENST00000442201.6:c.609+39G>T	ENSP00000405708.2:n.609+39G>T
ENST00000476379.5:c.609+39G>T	ENSP00000417960.1:n.609+39G>T
NM_181426.1:c.609+39G>T	NP_852091.1:n.609+39G>T
NM_181426.2:c.609+39G>T MANE Select	NP_852091.1:n.609+39G>T