Canonical Allele Identifier: CA2556109623

Gene: CCDC170

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151611982_151611983insTCTAG , CM000668.2:g.151611982_151611983insTCTAG	GRCh38
NC_000006.11:g.151933117_151933118insTCTAG , CM000668.1:g.151933117_151933118insTCTAG	GRCh37
NC_000006.10:g.151974810_151974811insTCTAG	NCBI36
NG_021198.1:g.122943_122944insTCTAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1711-3461_1711-3460insTCTAG MANE Select	ENSP00000239374.6:n.1711-3461_1711-3460insTCTAG
ENST00000239374.7:c.1711-3461_1711-3460insTCTAG	ENSP00000239374.6:n.1711-3461_1711-3460insTCTAG
ENST00000537358.1:n.497-3461_497-3460insTCTAG
NM_025059.3:c.1711-3461_1711-3460insTCTAG	NP_079335.2:n.1711-3461_1711-3460insTCTAG
XM_011536147.1:c.1729-3461_1729-3460insTCTAG	XP_011534449.1:n.1729-3461_1729-3460insTCTAG
XM_011536148.1:c.1528-3461_1528-3460insTCTAG	XP_011534450.1:n.1528-3461_1528-3460insTCTAG
XM_011536147.2:c.1729-3461_1729-3460insTCTAG	XP_011534449.1:n.1729-3461_1729-3460insTCTAG
XM_011536148.2:c.1528-3461_1528-3460insTCTAG	XP_011534450.1:n.1528-3461_1528-3460insTCTAG
XR_001743865.1:n.130-711_130-710insCTAGA
NM_025059.4:c.1711-3461_1711-3460insTCTAG MANE Select	NP_079335.2:n.1711-3461_1711-3460insTCTAG