Canonical Allele Identifier: CA45685124
Gene: TMEM178A HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs17024218

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.39712396T>C , CM000664.2:g.39712396T>C GRCh38
NC_000002.11:g.39939536T>C , CM000664.1:g.39939536T>C GRCh37
NC_000002.10:g.39793040T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NM_001167959.1:c.107-4614T>C VV NP_001161431.1:p.=
NM_152390.2:c.653-4614T>C VV NP_689603.2:p.=
XM_005264144.1:c.515-4614T>C XP_005264201.1:p.=
XM_005264145.1:c.401-4614T>C XP_005264202.1:p.=
XM_017003369.1:c.*854T>C XP_016858858.1:p.=
XM_017003370.2:c.107-4614T>C XP_016858859.1:p.=
XM_017003371.1:c.107-4614T>C XP_016858860.1:p.=
XM_024452702.1:c.401-22833T>C XP_024308470.1:p.=
XM_024452703.1:c.107-4614T>C XP_024308471.1:p.=
XM_024452704.1:c.107-4614T>C XP_024308472.1:p.=
XM_024452705.1:c.107-4614T>C XP_024308473.1:p.=
NM_152390.3:c.653-4614T>C VV MANE Preferred NP_689603.2:p.=
ENST00000281961.2:c.653-4614T>C ENSP00000281961.2:p.=
ENST00000413011.5:n.372-4614T>C
ENST00000482239.5:n.396-4614T>C
ENST00000495402.1:n.432-4614T>C
ENST00000618232.1:c.*42-4614T>C ENSP00000477622.1:p.=