Canonical Allele Identifier: CA355299664

Gene: CCDC39

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180652267C>A , CM000665.2:g.180652267C>A	GRCh38
NC_000003.11:g.180370055C>A , CM000665.1:g.180370055C>A	GRCh37
NC_000003.10:g.181852749C>A	NCBI36
NG_029581.1:g.32229G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_181426.2:c.931-1G>T MANE Select	NP_852091.1:n.931-1G>T
ENST00000476379.6:c.931-1G>T MANE Select	ENSP00000417960.2:n.931-1G>T
NM_181426.1:c.931-1G>T	NP_852091.1:n.931-1G>T
ENST00000442201.6:c.931-1G>T	ENSP00000405708.2:n.931-1G>T
ENST00000476379.5:c.931-1G>T	ENSP00000417960.1:n.931-1G>T
ENST00000650641.1:n.818-1G>T
ENST00000650889.1:n.1322-1G>T
ENST00000651046.1:c.739-1G>T	ENSP00000499175.1:n.739-1G>T
ENST00000651818.1:n.881-1G>T
ENST00000651922.1:n.255G>T
ENST00000652024.1:n.830-1G>T
ENST00000652408.1:n.1068-1G>T