Canonical Allele Identifier: CA362701565
Gene: TFAP2A HGNC NCBI
TFAP2A-AS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10404640A>G , CM000668.2:g.10404640A>G GRCh38
NC_000006.11:g.10404873A>G , CM000668.1:g.10404873A>G GRCh37
NC_000006.10:g.10512859A>G NCBI36
NG_016151.1:g.19925T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379608.9:c.614T>C (TFAP2A) ENSP00000368928.3:p.Phe205Ser
ENST00000379613.10:c.638T>C (TFAP2A) MANE Select ENSP00000368933.5:p.Phe213Ser
ENST00000482890.6:c.638T>C (TFAP2A) ENSP00000418541.2:p.Phe213Ser
ENST00000488193.7:c.*129T>C (TFAP2A) ENSP00000419823.3:n.*129T>C
ENST00000498450.3:c.203T>C (TFAP2A) ENSP00000419961.3:p.Phe68Ser
ENST00000319516.8:c.620T>C (TFAP2A) ENSP00000316516.4:p.Phe207Ser
ENST00000379608.7:c.614T>C (TFAP2A) ENSP00000368928.3:p.Phe205Ser
ENST00000379613.7:c.638T>C (TFAP2A) ENSP00000368933.3:p.Phe213Ser
ENST00000466073.5:c.632T>C (TFAP2A) ENSP00000417495.1:p.Phe211Ser
ENST00000475264.5:c.346T>C (TFAP2A)
ENST00000478375.5:n.632T>C (TFAP2A)
ENST00000482890.5:c.632T>C (TFAP2A) ENSP00000418541.1:p.Phe211Ser
ENST00000488193.5:c.*129T>C (TFAP2A) ENSP00000419823.1:n.*129T>C
ENST00000489805.5:c.*129T>C (TFAP2A) ENSP00000420568.1:n.*129T>C
ENST00000490875.5:n.874T>C (TFAP2A)
ENST00000497266.5:n.603T>C (TFAP2A)
ENST00000498450.1:c.203T>C (TFAP2A) ENSP00000419961.1:p.Phe68Ser
NM_001032280.2:c.614T>C (TFAP2A) NP_001027451.1:p.Phe205Ser
NM_001042425.1:c.620T>C (TFAP2A) NP_001035890.1:p.Phe207Ser
NM_003220.2:c.632T>C (TFAP2A) NP_003211.1:p.Phe211Ser
XM_006715175.2:c.767T>C (TFAP2A) XP_006715238.1:p.Phe256Ser
XM_011514833.1:c.482T>C (TFAP2A) XP_011513135.1:p.Phe161Ser
NR_145448.1:n.139A>G (TFAP2A-AS2)
XM_011514833.2:c.482T>C (TFAP2A) XP_011513135.1:p.Phe161Ser
XM_017011232.1:c.878T>C (TFAP2A) XP_016866721.1:p.Phe293Ser
NM_003220.3:c.632T>C (TFAP2A) NP_003211.1:p.Phe211Ser
NM_001032280.3:c.614T>C (TFAP2A) NP_001027451.1:p.Phe205Ser
NM_001042425.2:c.620T>C (TFAP2A) NP_001035890.1:p.Phe207Ser
NM_001372066.1:c.638T>C (TFAP2A) MANE Select NP_001358995.1:p.Phe213Ser
NM_001042425.3:c.620T>C (TFAP2A) NP_001035890.1:p.Phe207Ser