Canonical Allele Identifier: CA1672965849

Gene: CCDC170

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151618116_151618117delinsAC , CM000668.2:g.151618116_151618117delinsAC	GRCh38
NC_000006.11:g.151939251_151939252delinsAC , CM000668.1:g.151939251_151939252delinsAC	GRCh37
NC_000006.10:g.151980944_151980945delinsAC	NCBI36
NG_021198.1:g.129077_129078delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.2117_2118delinsAC MANE Select	ENSP00000239374.6:p.His706=
ENST00000239374.7:c.2117_2118delinsAC	ENSP00000239374.6:p.His706=
NM_025059.3:c.2117_2118delinsAC	NP_079335.2:p.His706=
XM_011536147.1:c.2135_2136delinsAC	XP_011534449.1:p.His712=
XM_011536148.1:c.1934_1935delinsAC	XP_011534450.1:p.His645=
XM_011536147.2:c.2135_2136delinsAC	XP_011534449.1:p.His712=
XM_011536148.2:c.1934_1935delinsAC	XP_011534450.1:p.His645=
NM_025059.4:c.2117_2118delinsAC MANE Select	NP_079335.2:p.His706=