Canonical Allele Identifier: CA1672962600

Gene: CCDC170

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615617G= , CM000668.2:g.151615617G=	GRCh38
NC_000006.11:g.151936752G= , CM000668.1:g.151936752G=	GRCh37
NC_000006.10:g.151978445G=	NCBI36
NG_021198.1:g.126578G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1885G= MANE Select	ENSP00000239374.6:p.Val629=
ENST00000239374.7:c.1885G=	ENSP00000239374.6:p.Val629=
NM_025059.3:c.1885G=	NP_079335.2:p.Val629=
XM_011536147.1:c.1903G=	XP_011534449.1:p.Val635=
XM_011536148.1:c.1702G=	XP_011534450.1:p.Val568=
XM_011536147.2:c.1903G=	XP_011534449.1:p.Val635=
XM_011536148.2:c.1702G=	XP_011534450.1:p.Val568=
XR_001743865.1:n.129+1104C=
NM_025059.4:c.1885G= MANE Select	NP_079335.2:p.Val629=