Canonical Allele Identifier: CA5176484

Gene: TMEM245

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.109033376G>C , CM000671.2:g.109033376G>C	GRCh38
NC_000009.11:g.111795656G>C , CM000671.1:g.111795656G>C	GRCh37
NC_000009.10:g.110835477G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_032012.4:c.2525C>G MANE Select	NP_114401.2:p.Ala842Gly
ENST00000374586.8:c.2525C>G MANE Select	ENSP00000363714.3:p.Ala842Gly
NM_032012.3:c.2525C>G	NP_114401.2:p.Ala842Gly
ENST00000374586.7:c.2525C>G	ENSP00000363714.3:p.Ala842Gly
ENST00000413712.6:c.1302C>G
ENST00000413712.7:c.2501C>G	ENSP00000394798.3:p.Ala834Gly
ENST00000472207.5:n.1612C>G
ENST00000491854.1:c.*1097C>G	ENSP00000417842.1:n.*1097C>G
XM_011518446.1:c.2522C>G	XP_011516748.1:p.Ala841Gly
XM_011518446.2:c.2522C>G	XP_011516748.1:p.Ala841Gly
XM_011518447.1:c.2501C>G	XP_011516749.1:p.Ala834Gly
XM_011518448.1:c.2420C>G	XP_011516750.1:p.Ala807Gly
XM_011518449.1:c.2408C>G	XP_011516751.1:p.Ala803Gly
XM_011518449.2:c.2408C>G	XP_011516751.1:p.Ala803Gly
XM_011518450.1:c.2405C>G	XP_011516752.1:p.Ala802Gly
XM_011518451.1:c.2396C>G	XP_011516753.1:p.Ala799Gly
XM_011518452.1:c.2291C>G	XP_011516754.1:p.Ala764Gly
XM_011518452.2:c.2291C>G	XP_011516754.1:p.Ala764Gly
XM_017014571.1:c.2498C>G	XP_016870060.1:p.Ala833Gly
XM_017014572.1:c.2267C>G	XP_016870061.1:p.Ala756Gly
XR_930240.1:n.1391+10186G>C