Canonical Allele Identifier: CA362701721
Gene: TFAP2A HGNC NCBI
TFAP2A-AS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10404680C>A , CM000668.2:g.10404680C>A GRCh38
NC_000006.11:g.10404913C>A , CM000668.1:g.10404913C>A GRCh37
NC_000006.10:g.10512899C>A NCBI36
NG_016151.1:g.19885G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379608.9:c.574G>T (TFAP2A) ENSP00000368928.3:p.Asp192Tyr
ENST00000379613.10:c.598G>T (TFAP2A) MANE Select ENSP00000368933.5:p.Asp200Tyr
ENST00000482890.6:c.598G>T (TFAP2A) ENSP00000418541.2:p.Asp200Tyr
ENST00000488193.7:c.*89G>T (TFAP2A) ENSP00000419823.3:n.*89G>T
ENST00000498450.3:c.163G>T (TFAP2A) ENSP00000419961.3:p.Asp55Tyr
ENST00000319516.8:c.580G>T (TFAP2A) ENSP00000316516.4:p.Asp194Tyr
ENST00000379608.7:c.574G>T (TFAP2A) ENSP00000368928.3:p.Asp192Tyr
ENST00000379613.7:c.598G>T (TFAP2A) ENSP00000368933.3:p.Asp200Tyr
ENST00000466073.5:c.592G>T (TFAP2A) ENSP00000417495.1:p.Asp198Tyr
ENST00000473652.1:n.646G>T (TFAP2A)
ENST00000475264.5:c.306G>T (TFAP2A)
ENST00000478375.5:n.592G>T (TFAP2A)
ENST00000482890.5:c.592G>T (TFAP2A) ENSP00000418541.1:p.Asp198Tyr
ENST00000488193.5:c.*89G>T (TFAP2A) ENSP00000419823.1:n.*89G>T
ENST00000489805.5:c.*89G>T (TFAP2A) ENSP00000420568.1:n.*89G>T
ENST00000490875.5:n.834G>T (TFAP2A)
ENST00000497266.5:n.563G>T (TFAP2A)
ENST00000498450.1:c.163G>T (TFAP2A) ENSP00000419961.1:p.Asp55Tyr
NM_001032280.2:c.574G>T (TFAP2A) NP_001027451.1:p.Asp192Tyr
NM_001042425.1:c.580G>T (TFAP2A) NP_001035890.1:p.Asp194Tyr
NM_003220.2:c.592G>T (TFAP2A) NP_003211.1:p.Asp198Tyr
XM_006715175.2:c.727G>T (TFAP2A) XP_006715238.1:p.Asp243Tyr
XM_011514833.1:c.442G>T (TFAP2A) XP_011513135.1:p.Asp148Tyr
NR_145448.1:n.179C>A (TFAP2A-AS2)
XM_011514833.2:c.442G>T (TFAP2A) XP_011513135.1:p.Asp148Tyr
XM_017011232.1:c.838G>T (TFAP2A) XP_016866721.1:p.Asp280Tyr
NM_003220.3:c.592G>T (TFAP2A) NP_003211.1:p.Asp198Tyr
NM_001032280.3:c.574G>T (TFAP2A) NP_001027451.1:p.Asp192Tyr
NM_001042425.2:c.580G>T (TFAP2A) NP_001035890.1:p.Asp194Tyr
NM_001372066.1:c.598G>T (TFAP2A) MANE Select NP_001358995.1:p.Asp200Tyr
NM_001042425.3:c.580G>T (TFAP2A) NP_001035890.1:p.Asp194Tyr