Canonical Allele Identifier: CA134049023
Gene: TFAP2A HGNC NCBI
TFAP2A-AS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 829802
ClinVar RCV Id: RCV001029733
dbSNP Id: rs151344527

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10404520C>T , CM000668.2:g.10404520C>T GRCh38
NC_000006.11:g.10404753C>T , CM000668.1:g.10404753C>T GRCh37
NC_000006.10:g.10512739C>T NCBI36
NG_016151.1:g.20045G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000379608.9:c.734G>A (TFAP2A) ENSP00000368928.3:p.Gly245Glu
ENST00000379613.10:c.758G>A (TFAP2A) MANE Select ENSP00000368933.5:p.Gly253Glu
ENST00000482890.6:c.758G>A (TFAP2A) ENSP00000418541.2:p.Gly253Glu
ENST00000488193.7:c.*249G>A (TFAP2A) ENSP00000419823.3:n.*249G>A
ENST00000498450.3:c.323G>A (TFAP2A) ENSP00000419961.3:p.Gly108Glu
ENST00000319516.8:c.740G>A (TFAP2A) ENSP00000316516.4:p.Gly247Glu
ENST00000379608.7:c.734G>A (TFAP2A) ENSP00000368928.3:p.Gly245Glu
ENST00000379613.7:c.758G>A (TFAP2A) ENSP00000368933.3:p.Gly253Glu
ENST00000461628.5:c.75G>A (TFAP2A)
ENST00000466073.5:c.752G>A (TFAP2A) ENSP00000417495.1:p.Gly251Glu
ENST00000475264.5:c.466G>A (TFAP2A)
ENST00000478375.5:n.752G>A (TFAP2A)
ENST00000482890.5:c.752G>A (TFAP2A) ENSP00000418541.1:p.Gly251Glu
ENST00000488193.5:c.*249G>A (TFAP2A) ENSP00000419823.1:n.*249G>A
ENST00000489805.5:c.*249G>A (TFAP2A) ENSP00000420568.1:n.*249G>A
ENST00000497266.5:n.723G>A (TFAP2A)
ENST00000498450.1:c.323G>A (TFAP2A) ENSP00000419961.1:p.Gly108Glu
NM_001032280.2:c.734G>A (TFAP2A) NP_001027451.1:p.Gly245Glu
NM_001042425.1:c.740G>A (TFAP2A) NP_001035890.1:p.Gly247Glu
NM_003220.2:c.752G>A (TFAP2A) NP_003211.1:p.Gly251Glu
XM_006715175.2:c.887G>A (TFAP2A) XP_006715238.1:p.Gly296Glu
XM_011514833.1:c.602G>A (TFAP2A) XP_011513135.1:p.Gly201Glu
NR_145448.1:n.19C>T (TFAP2A-AS2)
XM_011514833.2:c.602G>A (TFAP2A) XP_011513135.1:p.Gly201Glu
XM_017011232.1:c.998G>A (TFAP2A) XP_016866721.1:p.Gly333Glu
NM_003220.3:c.752G>A (TFAP2A) NP_003211.1:p.Gly251Glu
NM_001032280.3:c.734G>A (TFAP2A) NP_001027451.1:p.Gly245Glu
NM_001042425.2:c.740G>A (TFAP2A) NP_001035890.1:p.Gly247Glu
NM_001372066.1:c.758G>A (TFAP2A) MANE Select NP_001358995.1:p.Gly253Glu
NM_001042425.3:c.740G>A (TFAP2A) NP_001035890.1:p.Gly247Glu