Canonical Allele Identifier: CA1372661921
Gene: TAFA1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.68363724A= , CM000665.2:g.68363724A= GRCh38
NC_000003.11:g.68412874A= , CM000665.1:g.68412874A= GRCh37
NC_000003.10:g.68495564A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_213609.4:c.119-53556A= MANE Select NP_998774.2:n.119-53556A=
ENST00000478136.6:c.119-53556A= MANE Select ENSP00000418575.1:n.119-53556A=
NM_001252216.1:c.119-53556A= NP_001239145.1:n.119-53556A=
NM_001252216.2:c.119-53556A= NP_001239145.1:n.119-53556A=
NM_213609.3:c.119-53556A= NP_998774.2:n.119-53556A=
ENST00000478136.5:c.119-53556A= ENSP00000418575.1:n.119-53556A=
ENST00000491017.1:n.507-53556A=
ENST00000496687.1:c.119-53556A= ENSP00000417496.1:n.119-53556A=
XM_017006386.1:c.119-53556A= XP_016861875.1:n.119-53556A=
XM_017006387.2:c.119-53556A= XP_016861876.1:n.119-53556A=
XM_017006388.1:c.119-53559A= XP_016861877.1:n.119-53559A=
XM_017006389.1:c.119-53559A= XP_016861878.1:n.119-53559A=
XM_017006390.1:c.119-53559A= XP_016861879.1:n.119-53559A=