Canonical Allele Identifier: CA2840224521

Gene: CCDC170

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151580313T>C , CM000668.2:g.151580313T>C	GRCh38
NC_000006.11:g.151901448T>C , CM000668.1:g.151901448T>C	GRCh37
NC_000006.10:g.151943141T>C	NCBI36
NG_021198.1:g.91274T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1093-5576T>C MANE Select	ENSP00000239374.6:n.1093-5576T>C
ENST00000239374.7:c.1093-5576T>C	ENSP00000239374.6:n.1093-5576T>C
NM_025059.3:c.1093-5576T>C	NP_079335.2:n.1093-5576T>C
XM_011536147.1:c.1111-5576T>C	XP_011534449.1:n.1111-5576T>C
XM_011536148.1:c.1110+6822T>C	XP_011534450.1:n.1110+6822T>C
XM_011536147.2:c.1111-5576T>C	XP_011534449.1:n.1111-5576T>C
XM_011536148.2:c.1110+6822T>C	XP_011534450.1:n.1110+6822T>C
NM_025059.4:c.1093-5576T>C MANE Select	NP_079335.2:n.1093-5576T>C