Canonical Allele Identifier: CA374417121

Gene: TMEM245

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.109119564G>T , CM000671.2:g.109119564G>T	GRCh38
NC_000009.11:g.111881844G>T , CM000671.1:g.111881844G>T	GRCh37
NC_000009.10:g.110921665G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000413712.7:c.350C>A	ENSP00000394798.3:p.Thr117Lys
ENST00000374586.8:c.350C>A MANE Select	ENSP00000363714.3:p.Thr117Lys
ENST00000374586.7:c.350C>A	ENSP00000363714.3:p.Thr117Lys
NM_032012.3:c.350C>A	NP_114401.2:p.Thr117Lys
XM_011518446.1:c.350C>A	XP_011516748.1:p.Thr117Lys
XM_011518447.1:c.350C>A	XP_011516749.1:p.Thr117Lys
XM_011518448.1:c.350C>A	XP_011516750.1:p.Thr117Lys
XM_011518449.1:c.350C>A	XP_011516751.1:p.Thr117Lys
XM_011518450.1:c.350C>A	XP_011516752.1:p.Thr117Lys
XM_011518451.1:c.350C>A	XP_011516753.1:p.Thr117Lys
XM_011518452.1:c.350C>A	XP_011516754.1:p.Thr117Lys
XM_011518446.2:c.350C>A	XP_011516748.1:p.Thr117Lys
XM_011518449.2:c.350C>A	XP_011516751.1:p.Thr117Lys
XM_011518452.2:c.350C>A	XP_011516754.1:p.Thr117Lys
XM_017014571.1:c.350C>A	XP_016870060.1:p.Thr117Lys
XM_017014572.1:c.350C>A	XP_016870061.1:p.Thr117Lys
NM_032012.4:c.350C>A MANE Select	NP_114401.2:p.Thr117Lys