Canonical Allele Identifier: CA1835462904

Gene: TTC39B

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.15283075A= , CM000671.2:g.15283075A=	GRCh38
NC_000009.11:g.15283073A= , CM000671.1:g.15283073A=	GRCh37
NC_000009.10:g.15273073A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000297615.10:c.43-15127T=	ENSP00000297615.6:n.43-15127T=
ENST00000380850.9:c.43-15127T=	ENSP00000370231.5:n.43-15127T=
ENST00000512701.7:c.43-15127T= MANE Select	ENSP00000422496.2:n.43-15127T=
ENST00000297615.9:c.241-15127T=	ENSP00000297615.5:n.241-15127T=
ENST00000380850.8:c.241-15127T=	ENSP00000370231.4:n.241-15127T=
ENST00000505732.5:n.278-15127T=
ENST00000506891.1:c.127-15127T=	ENSP00000427314.1:n.127-15127T=
ENST00000512701.6:c.241-15127T=	ENSP00000422496.1:n.241-15127T=
NM_001168339.1:c.241-15127T=	NP_001161811.1:n.241-15127T=
NM_001168340.1:c.241-15127T=	NP_001161812.1:n.241-15127T=
NM_001168341.1:c.241-15127T=	NP_001161813.1:n.241-15127T=
NM_152574.2:c.241-15127T=	NP_689787.2:n.241-15127T=
XM_011517733.1:c.241-15127T=	XP_011516035.1:n.241-15127T=
XM_017014310.1:c.-112-14612T=	XP_016869799.1:n.-112-14612T=
XM_017014311.1:c.-221-14612T=	XP_016869800.1:n.-221-14612T=
XM_024447422.1:c.-51-15127T=	XP_024303190.1:n.-51-15127T=
XR_001746190.1:n.278-15127T=
NM_001168339.2:c.43-15127T=	NP_001161811.2:n.43-15127T=
NM_001168340.2:c.43-15127T=	NP_001161812.2:n.43-15127T=
NM_001168341.2:c.43-15127T=	NP_001161813.2:n.43-15127T=
NM_152574.3:c.43-15127T= MANE Select	NP_689787.3:n.43-15127T=