Canonical Allele Identifier: CA571437264

Gene: CCDC170

Linked Data

• dbSNP Id: rs1262637406
• gnomAD v2: 6-151936821-CTAAA-C
• MyVariant Identifiers: chr6:g.151936822_151936825del (hg19) ; chr6:g.151615687_151615690del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615688_151615691del , CM000668.2:g.151615688_151615691del	GRCh38
NC_000006.11:g.151936823_151936826del , CM000668.1:g.151936823_151936826del	GRCh37
NC_000006.10:g.151978516_151978519del	NCBI36
NG_021198.1:g.126649_126652del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1947+9_1947+12del MANE Select	ENSP00000239374.6:n.1947+9_1947+12del
ENST00000239374.7:c.1947+9_1947+12del	ENSP00000239374.6:n.1947+9_1947+12del
NM_025059.3:c.1947+9_1947+12del	NP_079335.2:n.1947+9_1947+12del
XM_011536147.1:c.1965+9_1965+12del	XP_011534449.1:n.1965+9_1965+12del
XM_011536148.1:c.1764+9_1764+12del	XP_011534450.1:n.1764+9_1764+12del
XM_011536147.2:c.1965+9_1965+12del	XP_011534449.1:n.1965+9_1965+12del
XM_011536148.2:c.1764+9_1764+12del	XP_011534450.1:n.1764+9_1764+12del
XR_001743865.1:n.129+1031_129+1034del
NM_025059.4:c.1947+9_1947+12del MANE Select	NP_079335.2:n.1947+9_1947+12del