Canonical Allele Identifier: CA1672962730
Gene: CCDC170 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151615700_151615701delinsGA , CM000668.2:g.151615700_151615701delinsGA GRCh38
NC_000006.11:g.151936835_151936836delinsGA , CM000668.1:g.151936835_151936836delinsGA GRCh37
NC_000006.10:g.151978528_151978529delinsGA NCBI36
NG_021198.1:g.126661_126662delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.1947+21_1947+22delinsGA MANE Select ENSP00000239374.6:n.1947+21_1947+22delinsGA
ENST00000239374.7:c.1947+21_1947+22delinsGA ENSP00000239374.6:n.1947+21_1947+22delinsGA
NM_025059.3:c.1947+21_1947+22delinsGA NP_079335.2:n.1947+21_1947+22delinsGA
XM_011536147.1:c.1965+21_1965+22delinsGA XP_011534449.1:n.1965+21_1965+22delinsGA
XM_011536148.1:c.1764+21_1764+22delinsGA XP_011534450.1:n.1764+21_1764+22delinsGA
XM_011536147.2:c.1965+21_1965+22delinsGA XP_011534449.1:n.1965+21_1965+22delinsGA
XM_011536148.2:c.1764+21_1764+22delinsGA XP_011534450.1:n.1764+21_1764+22delinsGA
XR_001743865.1:n.129+1020_129+1021delinsTC
NM_025059.4:c.1947+21_1947+22delinsGA MANE Select NP_079335.2:n.1947+21_1947+22delinsGA