Canonical Allele Identifier: CA2545310354

Gene: CCDC170

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151611986_151611987insA , CM000668.2:g.151611986_151611987insA	GRCh38
NC_000006.11:g.151933121_151933122insA , CM000668.1:g.151933121_151933122insA	GRCh37
NC_000006.10:g.151974814_151974815insA	NCBI36
NG_021198.1:g.122947_122948insA

Transcript Alleles

HGVS	Amino-acid change
ENST00000239374.8:c.1711-3457_1711-3456insA MANE Select	ENSP00000239374.6:n.1711-3457_1711-3456insA
ENST00000239374.7:c.1711-3457_1711-3456insA	ENSP00000239374.6:n.1711-3457_1711-3456insA
ENST00000537358.1:n.497-3457_497-3456insA
NM_025059.3:c.1711-3457_1711-3456insA	NP_079335.2:n.1711-3457_1711-3456insA
XM_011536147.1:c.1729-3457_1729-3456insA	XP_011534449.1:n.1729-3457_1729-3456insA
XM_011536148.1:c.1528-3457_1528-3456insA	XP_011534450.1:n.1528-3457_1528-3456insA
XM_011536147.2:c.1729-3457_1729-3456insA	XP_011534449.1:n.1729-3457_1729-3456insA
XM_011536148.2:c.1528-3457_1528-3456insA	XP_011534450.1:n.1528-3457_1528-3456insA
XR_001743865.1:n.130-715_130-714insT
NM_025059.4:c.1711-3457_1711-3456insA MANE Select	NP_079335.2:n.1711-3457_1711-3456insA