Canonical Allele Identifier: CA1672962734
Gene: CCDC170 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615703_151615704delinsAC , CM000668.2:g.151615703_151615704delinsAC GRCh38
NC_000006.11:g.151936838_151936839delinsAC , CM000668.1:g.151936838_151936839delinsAC GRCh37
NC_000006.10:g.151978531_151978532delinsAC NCBI36
NG_021198.1:g.126664_126665delinsAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1947+24_1947+25delinsAC MANE Select ENSP00000239374.6:n.1947+24_1947+25delinsAC
ENST00000239374.7:c.1947+24_1947+25delinsAC ENSP00000239374.6:n.1947+24_1947+25delinsAC
NM_025059.3:c.1947+24_1947+25delinsAC NP_079335.2:n.1947+24_1947+25delinsAC
XM_011536147.1:c.1965+24_1965+25delinsAC XP_011534449.1:n.1965+24_1965+25delinsAC
XM_011536148.1:c.1764+24_1764+25delinsAC XP_011534450.1:n.1764+24_1764+25delinsAC
XM_011536147.2:c.1965+24_1965+25delinsAC XP_011534449.1:n.1965+24_1965+25delinsAC
XM_011536148.2:c.1764+24_1764+25delinsAC XP_011534450.1:n.1764+24_1764+25delinsAC
XR_001743865.1:n.129+1017_129+1018delinsGT
NM_025059.4:c.1947+24_1947+25delinsAC MANE Select NP_079335.2:n.1947+24_1947+25delinsAC