Canonical Allele Identifier: CA362701912
Gene: TFAP2A HGNC NCBI
TFAP2A-AS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10404721T>G , CM000668.2:g.10404721T>G GRCh38
NC_000006.11:g.10404954T>G , CM000668.1:g.10404954T>G GRCh37
NC_000006.10:g.10512940T>G NCBI36
NG_016151.1:g.19844A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379608.9:c.533A>C (TFAP2A) ENSP00000368928.3:p.Lys178Thr
ENST00000379613.10:c.557A>C (TFAP2A) MANE Select ENSP00000368933.5:p.Lys186Thr
ENST00000482890.6:c.557A>C (TFAP2A) ENSP00000418541.2:p.Lys186Thr
ENST00000488193.7:c.*48A>C (TFAP2A) ENSP00000419823.3:n.*48A>C
ENST00000498450.3:c.122A>C (TFAP2A) ENSP00000419961.3:p.Lys41Thr
ENST00000319516.8:c.539A>C (TFAP2A) ENSP00000316516.4:p.Lys180Thr
ENST00000379608.7:c.533A>C (TFAP2A) ENSP00000368928.3:p.Lys178Thr
ENST00000379613.7:c.557A>C (TFAP2A) ENSP00000368933.3:p.Lys186Thr
ENST00000466073.5:c.551A>C (TFAP2A) ENSP00000417495.1:p.Lys184Thr
ENST00000473652.1:n.605A>C (TFAP2A)
ENST00000475264.5:c.265A>C (TFAP2A)
ENST00000478375.5:n.551A>C (TFAP2A)
ENST00000482890.5:c.551A>C (TFAP2A) ENSP00000418541.1:p.Lys184Thr
ENST00000488193.5:c.*48A>C (TFAP2A) ENSP00000419823.1:n.*48A>C
ENST00000489805.5:c.*48A>C (TFAP2A) ENSP00000420568.1:n.*48A>C
ENST00000490875.5:n.793A>C (TFAP2A)
ENST00000497266.5:n.522A>C (TFAP2A)
ENST00000498450.1:c.122A>C (TFAP2A) ENSP00000419961.1:p.Lys41Thr
NM_001032280.2:c.533A>C (TFAP2A) NP_001027451.1:p.Lys178Thr
NM_001042425.1:c.539A>C (TFAP2A) NP_001035890.1:p.Lys180Thr
NM_003220.2:c.551A>C (TFAP2A) NP_003211.1:p.Lys184Thr
XM_006715175.2:c.686A>C (TFAP2A) XP_006715238.1:p.Lys229Thr
XM_011514833.1:c.401A>C (TFAP2A) XP_011513135.1:p.Lys134Thr
NR_145448.1:n.220T>G (TFAP2A-AS2)
XM_011514833.2:c.401A>C (TFAP2A) XP_011513135.1:p.Lys134Thr
XM_017011232.1:c.797A>C (TFAP2A) XP_016866721.1:p.Lys266Thr
NM_003220.3:c.551A>C (TFAP2A) NP_003211.1:p.Lys184Thr
NM_001032280.3:c.533A>C (TFAP2A) NP_001027451.1:p.Lys178Thr
NM_001042425.2:c.539A>C (TFAP2A) NP_001035890.1:p.Lys180Thr
NM_001372066.1:c.557A>C (TFAP2A) MANE Select NP_001358995.1:p.Lys186Thr
NM_001042425.3:c.539A>C (TFAP2A) NP_001035890.1:p.Lys180Thr