Canonical Allele Identifier: CA366067032

Gene: CCDC170

Linked Data

• MyVariant Identifiers: chr6:g.151936648A>C (hg19) ; chr6:g.151615513A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615513A>C , CM000668.2:g.151615513A>C	GRCh38
NC_000006.11:g.151936648A>C , CM000668.1:g.151936648A>C	GRCh37
NC_000006.10:g.151978341A>C	NCBI36
NG_021198.1:g.126474A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1781A>C MANE Select	ENSP00000239374.6:p.Lys594Thr
ENST00000239374.7:c.1781A>C	ENSP00000239374.6:p.Lys594Thr
ENST00000537358.1:n.567A>C
NM_025059.3:c.1781A>C	NP_079335.2:p.Lys594Thr
XM_011536147.1:c.1799A>C	XP_011534449.1:p.Lys600Thr
XM_011536148.1:c.1598A>C	XP_011534450.1:p.Lys533Thr
XM_011536147.2:c.1799A>C	XP_011534449.1:p.Lys600Thr
XM_011536148.2:c.1598A>C	XP_011534450.1:p.Lys533Thr
XR_001743865.1:n.129+1208T>G
NM_025059.4:c.1781A>C MANE Select	NP_079335.2:p.Lys594Thr