Canonical Allele Identifier: CA366067557

Gene: CCDC170

Linked Data

• MyVariant Identifiers: chr6:g.151936711C>G (hg19) ; chr6:g.151615576C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.151615576C>G , CM000668.2:g.151615576C>G	GRCh38
NC_000006.11:g.151936711C>G , CM000668.1:g.151936711C>G	GRCh37
NC_000006.10:g.151978404C>G	NCBI36
NG_021198.1:g.126537C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000239374.8:c.1844C>G MANE Select	ENSP00000239374.6:p.Ala615Gly
ENST00000239374.7:c.1844C>G	ENSP00000239374.6:p.Ala615Gly
NM_025059.3:c.1844C>G	NP_079335.2:p.Ala615Gly
XM_011536147.1:c.1862C>G	XP_011534449.1:p.Ala621Gly
XM_011536148.1:c.1661C>G	XP_011534450.1:p.Ala554Gly
XM_011536147.2:c.1862C>G	XP_011534449.1:p.Ala621Gly
XM_011536148.2:c.1661C>G	XP_011534450.1:p.Ala554Gly
XR_001743865.1:n.129+1145G>C
NM_025059.4:c.1844C>G MANE Select	NP_079335.2:p.Ala615Gly