Canonical Allele Identifier: CA2773571652

Gene: CCDC170

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615644_151615645insCCAAACACACCCAACAC , CM000668.2:g.151615644_151615645insCCAAACACACCCAACAC	GRCh38
NC_000006.11:g.151936779_151936780insCCAAACACACCCAACAC , CM000668.1:g.151936779_151936780insCCAAACACACCCAACAC	GRCh37
NC_000006.10:g.151978472_151978473insCCAAACACACCCAACAC	NCBI36
NG_021198.1:g.126605_126606insCCAAACACACCCAACAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1912_1913insCCAAACACACCCAACAC MANE Select	ENSP00000239374.6:p.Lys638ThrfsTer30
ENST00000239374.7:c.1912_1913insCCAAACACACCCAACAC	ENSP00000239374.6:p.Lys638ThrfsTer30
NM_025059.3:c.1912_1913insCCAAACACACCCAACAC	NP_079335.2:p.Lys638ThrfsTer30
XM_011536147.1:c.1930_1931insCCAAACACACCCAACAC	XP_011534449.1:p.Lys644ThrfsTer30
XM_011536148.1:c.1729_1730insCCAAACACACCCAACAC	XP_011534450.1:p.Lys577ThrfsTer30
XM_011536147.2:c.1930_1931insCCAAACACACCCAACAC	XP_011534449.1:p.Lys644ThrfsTer30
XM_011536148.2:c.1729_1730insCCAAACACACCCAACAC	XP_011534450.1:p.Lys577ThrfsTer30
XR_001743865.1:n.129+1076_129+1077insGTGTTGGGTGTGTTTGG
NM_025059.4:c.1912_1913insCCAAACACACCCAACAC MANE Select	NP_079335.2:p.Lys638ThrfsTer30