Canonical Allele Identifier: CA452969757

Gene: CCDC170

Linked Data

• MyVariant Identifiers: chr6:g.151936751G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615616G>C , CM000668.2:g.151615616G>C	GRCh38
NC_000006.11:g.151936751G>C , CM000668.1:g.151936751G>C	GRCh37
NC_000006.10:g.151978444G>C	NCBI36
NG_021198.1:g.126577G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1884G>C MANE Select	ENSP00000239374.6:p.Val628=
ENST00000239374.7:c.1884G>C	ENSP00000239374.6:p.Val628=
NM_025059.3:c.1884G>C	NP_079335.2:p.Val628=
XM_011536147.1:c.1902G>C	XP_011534449.1:p.Val634=
XM_011536148.1:c.1701G>C	XP_011534450.1:p.Val567=
XM_011536147.2:c.1902G>C	XP_011534449.1:p.Val634=
XM_011536148.2:c.1701G>C	XP_011534450.1:p.Val567=
XR_001743865.1:n.129+1105C>G
NM_025059.4:c.1884G>C MANE Select	NP_079335.2:p.Val628=