Canonical Allele Identifier: CA2680800910

Gene: CCDC170

Linked Data

• gnomAD v4: 6-151615770-T-TA

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615776dup , CM000668.2:g.151615776dup	GRCh38
NC_000006.11:g.151936911dup , CM000668.1:g.151936911dup	GRCh37
NC_000006.10:g.151978604dup	NCBI36
NG_021198.1:g.126737dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1947+97dup MANE Select	ENSP00000239374.6:n.1947+97dup
ENST00000239374.7:c.1947+97dup	ENSP00000239374.6:n.1947+97dup
NM_025059.3:c.1947+97dup	NP_079335.2:n.1947+97dup
XM_011536147.1:c.1965+97dup	XP_011534449.1:n.1965+97dup
XM_011536148.1:c.1764+97dup	XP_011534450.1:n.1764+97dup
XM_011536147.2:c.1965+97dup	XP_011534449.1:n.1965+97dup
XM_011536148.2:c.1764+97dup	XP_011534450.1:n.1764+97dup
XR_001743865.1:n.129+950dup
NM_025059.4:c.1947+97dup MANE Select	NP_079335.2:n.1947+97dup