Canonical Allele Identifier: CA189402734

Gene: TTC39B

Linked Data

• dbSNP Id: rs1011318507
• MyVariant Identifiers: chr9:g.15283140T>C (hg19) ; chr9:g.15283142T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.15283142T>C , CM000671.2:g.15283142T>C	GRCh38
NC_000009.11:g.15283140T>C , CM000671.1:g.15283140T>C	GRCh37
NC_000009.10:g.15273140T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000297615.10:c.43-15194A>G	ENSP00000297615.6:n.43-15194A>G
ENST00000380850.9:c.43-15194A>G	ENSP00000370231.5:n.43-15194A>G
ENST00000512701.7:c.43-15194A>G MANE Select	ENSP00000422496.2:n.43-15194A>G
ENST00000297615.9:c.241-15194A>G	ENSP00000297615.5:n.241-15194A>G
ENST00000380850.8:c.241-15194A>G	ENSP00000370231.4:n.241-15194A>G
ENST00000505732.5:n.278-15194A>G
ENST00000506891.1:c.127-15194A>G	ENSP00000427314.1:n.127-15194A>G
ENST00000512701.6:c.241-15194A>G	ENSP00000422496.1:n.241-15194A>G
NM_001168339.1:c.241-15194A>G	NP_001161811.1:n.241-15194A>G
NM_001168340.1:c.241-15194A>G	NP_001161812.1:n.241-15194A>G
NM_001168341.1:c.241-15194A>G	NP_001161813.1:n.241-15194A>G
NM_152574.2:c.241-15194A>G	NP_689787.2:n.241-15194A>G
XM_011517733.1:c.241-15194A>G	XP_011516035.1:n.241-15194A>G
XM_017014310.1:c.-112-14679A>G	XP_016869799.1:n.-112-14679A>G
XM_017014311.1:c.-221-14679A>G	XP_016869800.1:n.-221-14679A>G
XM_024447422.1:c.-51-15194A>G	XP_024303190.1:n.-51-15194A>G
XR_001746190.1:n.278-15194A>G
NM_001168339.2:c.43-15194A>G	NP_001161811.2:n.43-15194A>G
NM_001168340.2:c.43-15194A>G	NP_001161812.2:n.43-15194A>G
NM_001168341.2:c.43-15194A>G	NP_001161813.2:n.43-15194A>G
NM_152574.3:c.43-15194A>G MANE Select	NP_689787.3:n.43-15194A>G