Canonical Allele Identifier: CA362701898
Gene: TFAP2A HGNC NCBI
TFAP2A-AS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10404718G>A , CM000668.2:g.10404718G>A GRCh38
NC_000006.11:g.10404951G>A , CM000668.1:g.10404951G>A GRCh37
NC_000006.10:g.10512937G>A NCBI36
NG_016151.1:g.19847C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379608.9:c.536C>T (TFAP2A) ENSP00000368928.3:p.Ser179Phe
ENST00000379613.10:c.560C>T (TFAP2A) MANE Select ENSP00000368933.5:p.Ser187Phe
ENST00000482890.6:c.560C>T (TFAP2A) ENSP00000418541.2:p.Ser187Phe
ENST00000488193.7:c.*51C>T (TFAP2A) ENSP00000419823.3:n.*51C>T
ENST00000498450.3:c.125C>T (TFAP2A) ENSP00000419961.3:p.Ser42Phe
ENST00000319516.8:c.542C>T (TFAP2A) ENSP00000316516.4:p.Ser181Phe
ENST00000379608.7:c.536C>T (TFAP2A) ENSP00000368928.3:p.Ser179Phe
ENST00000379613.7:c.560C>T (TFAP2A) ENSP00000368933.3:p.Ser187Phe
ENST00000466073.5:c.554C>T (TFAP2A) ENSP00000417495.1:p.Ser185Phe
ENST00000473652.1:n.608C>T (TFAP2A)
ENST00000475264.5:c.268C>T (TFAP2A)
ENST00000478375.5:n.554C>T (TFAP2A)
ENST00000482890.5:c.554C>T (TFAP2A) ENSP00000418541.1:p.Ser185Phe
ENST00000488193.5:c.*51C>T (TFAP2A) ENSP00000419823.1:n.*51C>T
ENST00000489805.5:c.*51C>T (TFAP2A) ENSP00000420568.1:n.*51C>T
ENST00000490875.5:n.796C>T (TFAP2A)
ENST00000497266.5:n.525C>T (TFAP2A)
ENST00000498450.1:c.125C>T (TFAP2A) ENSP00000419961.1:p.Ser42Phe
NM_001032280.2:c.536C>T (TFAP2A) NP_001027451.1:p.Ser179Phe
NM_001042425.1:c.542C>T (TFAP2A) NP_001035890.1:p.Ser181Phe
NM_003220.2:c.554C>T (TFAP2A) NP_003211.1:p.Ser185Phe
XM_006715175.2:c.689C>T (TFAP2A) XP_006715238.1:p.Ser230Phe
XM_011514833.1:c.404C>T (TFAP2A) XP_011513135.1:p.Ser135Phe
NR_145448.1:n.217G>A (TFAP2A-AS2)
XM_011514833.2:c.404C>T (TFAP2A) XP_011513135.1:p.Ser135Phe
XM_017011232.1:c.800C>T (TFAP2A) XP_016866721.1:p.Ser267Phe
NM_003220.3:c.554C>T (TFAP2A) NP_003211.1:p.Ser185Phe
NM_001032280.3:c.536C>T (TFAP2A) NP_001027451.1:p.Ser179Phe
NM_001042425.2:c.542C>T (TFAP2A) NP_001035890.1:p.Ser181Phe
NM_001372066.1:c.560C>T (TFAP2A) MANE Select NP_001358995.1:p.Ser187Phe
NM_001042425.3:c.542C>T (TFAP2A) NP_001035890.1:p.Ser181Phe