Canonical Allele Identifier: CA1672962613

Gene: CCDC170

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615625T= , CM000668.2:g.151615625T=	GRCh38
NC_000006.11:g.151936760T= , CM000668.1:g.151936760T=	GRCh37
NC_000006.10:g.151978453T=	NCBI36
NG_021198.1:g.126586T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1893T= MANE Select	ENSP00000239374.6:p.Ser631=
ENST00000239374.7:c.1893T=	ENSP00000239374.6:p.Ser631=
NM_025059.3:c.1893T=	NP_079335.2:p.Ser631=
XM_011536147.1:c.1911T=	XP_011534449.1:p.Ser637=
XM_011536148.1:c.1710T=	XP_011534450.1:p.Ser570=
XM_011536147.2:c.1911T=	XP_011534449.1:p.Ser637=
XM_011536148.2:c.1710T=	XP_011534450.1:p.Ser570=
XR_001743865.1:n.129+1096A=
NM_025059.4:c.1893T= MANE Select	NP_079335.2:p.Ser631=