Canonical Allele Identifier: CA1835466569

Gene: TTC39B

Linked Data

• dbSNP Id: rs1824106210

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.15289589A>T , CM000671.2:g.15289589A>T	GRCh38
NC_000009.11:g.15289587A>T , CM000671.1:g.15289587A>T	GRCh37
NC_000009.10:g.15279587A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000297615.10:c.42+17495T>A	ENSP00000297615.6:n.42+17495T>A
ENST00000380850.9:c.42+17495T>A	ENSP00000370231.5:n.42+17495T>A
ENST00000512701.7:c.42+17495T>A MANE Select	ENSP00000422496.2:n.42+17495T>A
ENST00000297615.9:c.240+17495T>A	ENSP00000297615.5:n.240+17495T>A
ENST00000380850.8:c.240+17495T>A	ENSP00000370231.4:n.240+17495T>A
ENST00000505732.5:n.277+17495T>A
ENST00000506891.1:c.126+17495T>A	ENSP00000427314.1:n.126+17495T>A
ENST00000512701.6:c.240+17495T>A	ENSP00000422496.1:n.240+17495T>A
NM_001168339.1:c.240+17495T>A	NP_001161811.1:n.240+17495T>A
NM_001168340.1:c.240+17495T>A	NP_001161812.1:n.240+17495T>A
NM_001168341.1:c.240+17495T>A	NP_001161813.1:n.240+17495T>A
NM_152574.2:c.240+17495T>A	NP_689787.2:n.240+17495T>A
XM_011517733.1:c.240+17495T>A	XP_011516035.1:n.240+17495T>A
XM_017014310.1:c.-113+9761T>A	XP_016869799.1:n.-113+9761T>A
XM_017014311.1:c.-222+9761T>A	XP_016869800.1:n.-222+9761T>A
XM_024447422.1:c.-52+9761T>A	XP_024303190.1:n.-52+9761T>A
XR_001746190.1:n.277+17495T>A
NM_001168339.2:c.42+17495T>A	NP_001161811.2:n.42+17495T>A
NM_001168340.2:c.42+17495T>A	NP_001161812.2:n.42+17495T>A
NM_001168341.2:c.42+17495T>A	NP_001161813.2:n.42+17495T>A
NM_152574.3:c.42+17495T>A MANE Select	NP_689787.3:n.42+17495T>A