Canonical Allele Identifier: CA1609976818

Gene: TFAP2A TFAP2A-AS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404730G= , CM000668.2:g.10404730G=	GRCh38
NC_000006.11:g.10404963G= , CM000668.1:g.10404963G=	GRCh37
NC_000006.10:g.10512949G=	NCBI36
NG_016151.1:g.19835C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.524C= (TFAP2A)	ENSP00000368928.3:p.Ser175=
ENST00000379613.10:c.548C= (TFAP2A) MANE Select	ENSP00000368933.5:p.Ser183=
ENST00000482890.6:c.548C= (TFAP2A)	ENSP00000418541.2:p.Ser183=
ENST00000488193.7:c.*39C= (TFAP2A)	ENSP00000419823.3:n.*39C=
ENST00000498450.3:c.113C= (TFAP2A)	ENSP00000419961.3:p.Ser38=
ENST00000319516.8:c.530C= (TFAP2A)	ENSP00000316516.4:p.Ser177=
ENST00000379608.7:c.524C= (TFAP2A)	ENSP00000368928.3:p.Ser175=
ENST00000379613.7:c.548C= (TFAP2A)	ENSP00000368933.3:p.Ser183=
ENST00000466073.5:c.542C= (TFAP2A)	ENSP00000417495.1:p.Ser181=
ENST00000473652.1:n.596C= (TFAP2A)
ENST00000475264.5:c.256C= (TFAP2A)
ENST00000478375.5:n.542C= (TFAP2A)
ENST00000482890.5:c.542C= (TFAP2A)	ENSP00000418541.1:p.Ser181=
ENST00000488193.5:c.*39C= (TFAP2A)	ENSP00000419823.1:n.*39C=
ENST00000489805.5:c.*39C= (TFAP2A)	ENSP00000420568.1:n.*39C=
ENST00000490875.5:n.784C= (TFAP2A)
ENST00000497266.5:n.513C= (TFAP2A)
ENST00000498450.1:c.113C= (TFAP2A)	ENSP00000419961.1:p.Ser38=
NM_001032280.2:c.524C= (TFAP2A)	NP_001027451.1:p.Ser175=
NM_001042425.1:c.530C= (TFAP2A)	NP_001035890.1:p.Ser177=
NM_003220.2:c.542C= (TFAP2A)	NP_003211.1:p.Ser181=
XM_006715175.2:c.677C= (TFAP2A)	XP_006715238.1:p.Ser226=
XM_011514833.1:c.392C= (TFAP2A)	XP_011513135.1:p.Ser131=
NR_145448.1:n.229G= (TFAP2A-AS2)
XM_011514833.2:c.392C= (TFAP2A)	XP_011513135.1:p.Ser131=
XM_017011232.1:c.788C= (TFAP2A)	XP_016866721.1:p.Ser263=
NM_003220.3:c.542C= (TFAP2A)	NP_003211.1:p.Ser181=
NM_001032280.3:c.524C= (TFAP2A)	NP_001027451.1:p.Ser175=
NM_001042425.2:c.530C= (TFAP2A)	NP_001035890.1:p.Ser177=
NM_001372066.1:c.548C= (TFAP2A) MANE Select	NP_001358995.1:p.Ser183=
NM_001042425.3:c.530C= (TFAP2A)	NP_001035890.1:p.Ser177=