Canonical Allele Identifier: CA903358505

Gene: CCDC39

Linked Data

• dbSNP Id: rs1387412810
• MyVariant Identifiers: chr3:g.180377815T>C (hg19) ; chr3:g.180660027T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.180660027T>C , CM000665.2:g.180660027T>C	GRCh38
NC_000003.11:g.180377815T>C , CM000665.1:g.180377815T>C	GRCh37
NC_000003.10:g.181860509T>C	NCBI36
NG_029581.1:g.24469A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000476379.6:c.517-258A>G MANE Select	ENSP00000417960.2:n.517-258A>G
ENST00000650641.1:n.596-258A>G
ENST00000650889.1:n.689-258A>G
ENST00000651046.1:c.517-258A>G	ENSP00000499175.1:n.517-258A>G
ENST00000651818.1:n.659-258A>G
ENST00000652024.1:n.608-258A>G
ENST00000652408.1:n.654-258A>G
ENST00000442201.6:c.517-258A>G	ENSP00000405708.2:n.517-258A>G
ENST00000476379.5:c.517-258A>G	ENSP00000417960.1:n.517-258A>G
NM_181426.1:c.517-258A>G	NP_852091.1:n.517-258A>G
NM_181426.2:c.517-258A>G MANE Select	NP_852091.1:n.517-258A>G