Canonical Allele Identifier: CA2680800822

Gene: CCDC170

Linked Data

• gnomAD v4: 6-151615402-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615402T>C , CM000668.2:g.151615402T>C	GRCh38
NC_000006.11:g.151936537T>C , CM000668.1:g.151936537T>C	GRCh37
NC_000006.10:g.151978230T>C	NCBI36
NG_021198.1:g.126363T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1711-41T>C MANE Select	ENSP00000239374.6:n.1711-41T>C
ENST00000239374.7:c.1711-41T>C	ENSP00000239374.6:n.1711-41T>C
ENST00000537358.1:n.497-41T>C
NM_025059.3:c.1711-41T>C	NP_079335.2:n.1711-41T>C
XM_011536147.1:c.1729-41T>C	XP_011534449.1:n.1729-41T>C
XM_011536148.1:c.1528-41T>C	XP_011534450.1:n.1528-41T>C
XM_011536147.2:c.1729-41T>C	XP_011534449.1:n.1729-41T>C
XM_011536148.2:c.1528-41T>C	XP_011534450.1:n.1528-41T>C
XR_001743865.1:n.129+1319A>G
NM_025059.4:c.1711-41T>C MANE Select	NP_079335.2:n.1711-41T>C