Canonical Allele Identifier: CA150160111

Gene: CCDC170

Linked Data

• dbSNP Id: rs1035450916
• MyVariant Identifiers: chr6:g.151901343A>T (hg19) ; chr6:g.151580208A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151580208A>T , CM000668.2:g.151580208A>T	GRCh38
NC_000006.11:g.151901343A>T , CM000668.1:g.151901343A>T	GRCh37
NC_000006.10:g.151943036A>T	NCBI36
NG_021198.1:g.91169A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000239374.8:c.1093-5681A>T MANE Select	ENSP00000239374.6:n.1093-5681A>T
ENST00000239374.7:c.1093-5681A>T	ENSP00000239374.6:n.1093-5681A>T
NM_025059.3:c.1093-5681A>T	NP_079335.2:n.1093-5681A>T
XM_011536147.1:c.1111-5681A>T	XP_011534449.1:n.1111-5681A>T
XM_011536148.1:c.1110+6717A>T	XP_011534450.1:n.1110+6717A>T
XM_011536147.2:c.1111-5681A>T	XP_011534449.1:n.1111-5681A>T
XM_011536148.2:c.1110+6717A>T	XP_011534450.1:n.1110+6717A>T
NM_025059.4:c.1093-5681A>T MANE Select	NP_079335.2:n.1093-5681A>T