Canonical Allele Identifier: CA1835462937

Gene: TTC39B

Linked Data

• dbSNP Id: rs1823830346

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.15283145A>T , CM000671.2:g.15283145A>T	GRCh38
NC_000009.11:g.15283143A>T , CM000671.1:g.15283143A>T	GRCh37
NC_000009.10:g.15273143A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000297615.10:c.43-15197T>A	ENSP00000297615.6:n.43-15197T>A
ENST00000380850.9:c.43-15197T>A	ENSP00000370231.5:n.43-15197T>A
ENST00000512701.7:c.43-15197T>A MANE Select	ENSP00000422496.2:n.43-15197T>A
ENST00000297615.9:c.241-15197T>A	ENSP00000297615.5:n.241-15197T>A
ENST00000380850.8:c.241-15197T>A	ENSP00000370231.4:n.241-15197T>A
ENST00000505732.5:n.278-15197T>A
ENST00000506891.1:c.127-15197T>A	ENSP00000427314.1:n.127-15197T>A
ENST00000512701.6:c.241-15197T>A	ENSP00000422496.1:n.241-15197T>A
NM_001168339.1:c.241-15197T>A	NP_001161811.1:n.241-15197T>A
NM_001168340.1:c.241-15197T>A	NP_001161812.1:n.241-15197T>A
NM_001168341.1:c.241-15197T>A	NP_001161813.1:n.241-15197T>A
NM_152574.2:c.241-15197T>A	NP_689787.2:n.241-15197T>A
XM_011517733.1:c.241-15197T>A	XP_011516035.1:n.241-15197T>A
XM_017014310.1:c.-112-14682T>A	XP_016869799.1:n.-112-14682T>A
XM_017014311.1:c.-221-14682T>A	XP_016869800.1:n.-221-14682T>A
XM_024447422.1:c.-51-15197T>A	XP_024303190.1:n.-51-15197T>A
XR_001746190.1:n.278-15197T>A
NM_001168339.2:c.43-15197T>A	NP_001161811.2:n.43-15197T>A
NM_001168340.2:c.43-15197T>A	NP_001161812.2:n.43-15197T>A
NM_001168341.2:c.43-15197T>A	NP_001161813.2:n.43-15197T>A
NM_152574.3:c.43-15197T>A MANE Select	NP_689787.3:n.43-15197T>A