Canonical Allele Identifier: CA1248203687
Gene: MTA3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.42754024A= , CM000664.2:g.42754024A= GRCh38
NC_000002.11:g.42981164A= , CM000664.1:g.42981164A= GRCh37
NC_000002.10:g.42834668A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000405094.2:c.*625A= MANE Select ENSP00000385823.1:n.*625A=
ENST00000405592.5:c.*625A= ENSP00000383973.1:n.*625A=
ENST00000406652.5:c.*625A= ENSP00000384249.1:n.*625A=
ENST00000409019.5:c.*708A= ENSP00000386763.1:n.*708A=
NM_001282755.1:c.*625A= NP_001269684.1:n.*625A=
NM_001282756.1:c.*625A= NP_001269685.1:n.*625A=
XM_005264456.2:c.*625A= XP_005264513.1:n.*625A=
XM_005264458.2:c.*625A= XP_005264515.1:n.*625A=
XM_005264459.2:c.*625A= XP_005264516.1:n.*625A=
XM_011533006.1:c.*625A= XP_011531308.1:n.*625A=
XR_939697.1:n.1791-29891A=
XR_939698.1:n.2441A=
NM_001330442.1:c.*625A= NP_001317371.1:n.*625A=
NM_001330443.1:c.*625A= NP_001317372.1:n.*625A=
NM_001330444.1:c.*625A= NP_001317373.1:n.*625A=
XM_024453019.1:c.*625A= XP_024308787.1:n.*625A=
XR_001738859.2:n.1794-29891A=
XR_001738860.2:n.2441A=
XR_939697.3:n.1794-29891A=
NM_001330442.2:c.*625A= MANE Select NP_001317371.1:n.*625A=
NM_001330443.2:c.*625A= NP_001317372.1:n.*625A=
NM_001330444.2:c.*625A= NP_001317373.1:n.*625A=
NM_001282755.2:c.*625A= NP_001269684.1:n.*625A=
NM_001282756.2:c.*625A= NP_001269685.1:n.*625A=