Canonical Allele Identifier: CA2680800898

Gene: CCDC170

Linked Data

• gnomAD v4: 6-151615752-TATTC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615755_151615758del , CM000668.2:g.151615755_151615758del	GRCh38
NC_000006.11:g.151936890_151936893del , CM000668.1:g.151936890_151936893del	GRCh37
NC_000006.10:g.151978583_151978586del	NCBI36
NG_021198.1:g.126716_126719del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1947+76_1947+79del MANE Select	ENSP00000239374.6:n.1947+76_1947+79del
ENST00000239374.7:c.1947+76_1947+79del	ENSP00000239374.6:n.1947+76_1947+79del
NM_025059.3:c.1947+76_1947+79del	NP_079335.2:n.1947+76_1947+79del
XM_011536147.1:c.1965+76_1965+79del	XP_011534449.1:n.1965+76_1965+79del
XM_011536148.1:c.1764+76_1764+79del	XP_011534450.1:n.1764+76_1764+79del
XM_011536147.2:c.1965+76_1965+79del	XP_011534449.1:n.1965+76_1965+79del
XM_011536148.2:c.1764+76_1764+79del	XP_011534450.1:n.1764+76_1764+79del
XR_001743865.1:n.129+965_129+968del
NM_025059.4:c.1947+76_1947+79del MANE Select	NP_079335.2:n.1947+76_1947+79del