Canonical Allele Identifier: CA2840263087

Gene: CCDC170

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151618220T>C , CM000668.2:g.151618220T>C	GRCh38
NC_000006.11:g.151939355T>C , CM000668.1:g.151939355T>C	GRCh37
NC_000006.10:g.151981048T>C	NCBI36
NG_021198.1:g.129181T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.*73T>C MANE Select	ENSP00000239374.6:n.*73T>C
ENST00000239374.7:c.*73T>C	ENSP00000239374.6:n.*73T>C
NM_025059.3:c.*73T>C	NP_079335.2:n.*73T>C
XM_011536147.1:c.*73T>C	XP_011534449.1:n.*73T>C
XM_011536148.1:c.*73T>C	XP_011534450.1:n.*73T>C
XM_011536147.2:c.*73T>C	XP_011534449.1:n.*73T>C
XM_011536148.2:c.*73T>C	XP_011534450.1:n.*73T>C
NM_025059.4:c.*73T>C MANE Select	NP_079335.2:n.*73T>C