Canonical Allele Identifier: CA1835466401
Gene: TTC39B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.15289278_15289279delinsTG , CM000671.2:g.15289278_15289279delinsTG GRCh38
NC_000009.11:g.15289276_15289277delinsTG , CM000671.1:g.15289276_15289277delinsTG GRCh37
NC_000009.10:g.15279276_15279277delinsTG NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000297615.10:c.42+17805_42+17806delinsCA ENSP00000297615.6:n.42+17805_42+17806delinsCA
ENST00000380850.9:c.42+17805_42+17806delinsCA ENSP00000370231.5:n.42+17805_42+17806delinsCA
ENST00000512701.7:c.42+17805_42+17806delinsCA MANE Select ENSP00000422496.2:n.42+17805_42+17806delinsCA
ENST00000297615.9:c.240+17805_240+17806delinsCA ENSP00000297615.5:n.240+17805_240+17806delinsCA
ENST00000380850.8:c.240+17805_240+17806delinsCA ENSP00000370231.4:n.240+17805_240+17806delinsCA
ENST00000505732.5:n.277+17805_277+17806delinsCA
ENST00000506891.1:c.126+17805_126+17806delinsCA ENSP00000427314.1:n.126+17805_126+17806delinsCA
ENST00000512701.6:c.240+17805_240+17806delinsCA ENSP00000422496.1:n.240+17805_240+17806delinsCA
NM_001168339.1:c.240+17805_240+17806delinsCA NP_001161811.1:n.240+17805_240+17806delinsCA
NM_001168340.1:c.240+17805_240+17806delinsCA NP_001161812.1:n.240+17805_240+17806delinsCA
NM_001168341.1:c.240+17805_240+17806delinsCA NP_001161813.1:n.240+17805_240+17806delinsCA
NM_152574.2:c.240+17805_240+17806delinsCA NP_689787.2:n.240+17805_240+17806delinsCA
XM_011517733.1:c.240+17805_240+17806delinsCA XP_011516035.1:n.240+17805_240+17806delinsCA
XM_017014310.1:c.-113+10071_-113+10072delinsCA XP_016869799.1:n.-113+10071_-113+10072delinsCA
XM_017014311.1:c.-222+10071_-222+10072delinsCA XP_016869800.1:n.-222+10071_-222+10072delinsCA
XM_024447422.1:c.-52+10071_-52+10072delinsCA XP_024303190.1:n.-52+10071_-52+10072delinsCA
XR_001746190.1:n.277+17805_277+17806delinsCA
NM_001168339.2:c.42+17805_42+17806delinsCA NP_001161811.2:n.42+17805_42+17806delinsCA
NM_001168340.2:c.42+17805_42+17806delinsCA NP_001161812.2:n.42+17805_42+17806delinsCA
NM_001168341.2:c.42+17805_42+17806delinsCA NP_001161813.2:n.42+17805_42+17806delinsCA
NM_152574.3:c.42+17805_42+17806delinsCA MANE Select NP_689787.3:n.42+17805_42+17806delinsCA