Canonical Allele Identifier: CA1672966051
Gene: CCDC170 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.151618283G= , CM000668.2:g.151618283G= GRCh38
NC_000006.11:g.151939418G= , CM000668.1:g.151939418G= GRCh37
NC_000006.10:g.151981111G= NCBI36
NG_021198.1:g.129244G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000239374.8:c.*136G= MANE Select ENSP00000239374.6:n.*136G=
ENST00000239374.7:c.*136G= ENSP00000239374.6:n.*136G=
NM_025059.3:c.*136G= NP_079335.2:n.*136G=
XM_011536147.1:c.*136G= XP_011534449.1:n.*136G=
XM_011536148.1:c.*136G= XP_011534450.1:n.*136G=
XM_011536147.2:c.*136G= XP_011534449.1:n.*136G=
XM_011536148.2:c.*136G= XP_011534450.1:n.*136G=
NM_025059.4:c.*136G= MANE Select NP_079335.2:n.*136G=
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