Canonical Allele Identifier: CA1609976793

Gene: TFAP2A TFAP2A-AS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404678G= , CM000668.2:g.10404678G=	GRCh38
NC_000006.11:g.10404911G= , CM000668.1:g.10404911G=	GRCh37
NC_000006.10:g.10512897G=	NCBI36
NG_016151.1:g.19887C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.576C= (TFAP2A)	ENSP00000368928.3:p.Asp192=
ENST00000379613.10:c.600C= (TFAP2A) MANE Select	ENSP00000368933.5:p.Asp200=
ENST00000482890.6:c.600C= (TFAP2A)	ENSP00000418541.2:p.Asp200=
ENST00000488193.7:c.*91C= (TFAP2A)	ENSP00000419823.3:n.*91C=
ENST00000498450.3:c.165C= (TFAP2A)	ENSP00000419961.3:p.Asp55=
ENST00000319516.8:c.582C= (TFAP2A)	ENSP00000316516.4:p.Asp194=
ENST00000379608.7:c.576C= (TFAP2A)	ENSP00000368928.3:p.Asp192=
ENST00000379613.7:c.600C= (TFAP2A)	ENSP00000368933.3:p.Asp200=
ENST00000466073.5:c.594C= (TFAP2A)	ENSP00000417495.1:p.Asp198=
ENST00000473652.1:n.648C= (TFAP2A)
ENST00000475264.5:c.308C= (TFAP2A)
ENST00000478375.5:n.594C= (TFAP2A)
ENST00000482890.5:c.594C= (TFAP2A)	ENSP00000418541.1:p.Asp198=
ENST00000488193.5:c.*91C= (TFAP2A)	ENSP00000419823.1:n.*91C=
ENST00000489805.5:c.*91C= (TFAP2A)	ENSP00000420568.1:n.*91C=
ENST00000490875.5:n.836C= (TFAP2A)
ENST00000497266.5:n.565C= (TFAP2A)
ENST00000498450.1:c.165C= (TFAP2A)	ENSP00000419961.1:p.Asp55=
NM_001032280.2:c.576C= (TFAP2A)	NP_001027451.1:p.Asp192=
NM_001042425.1:c.582C= (TFAP2A)	NP_001035890.1:p.Asp194=
NM_003220.2:c.594C= (TFAP2A)	NP_003211.1:p.Asp198=
XM_006715175.2:c.729C= (TFAP2A)	XP_006715238.1:p.Asp243=
XM_011514833.1:c.444C= (TFAP2A)	XP_011513135.1:p.Asp148=
NR_145448.1:n.177G= (TFAP2A-AS2)
XM_011514833.2:c.444C= (TFAP2A)	XP_011513135.1:p.Asp148=
XM_017011232.1:c.840C= (TFAP2A)	XP_016866721.1:p.Asp280=
NM_003220.3:c.594C= (TFAP2A)	NP_003211.1:p.Asp198=
NM_001032280.3:c.576C= (TFAP2A)	NP_001027451.1:p.Asp192=
NM_001042425.2:c.582C= (TFAP2A)	NP_001035890.1:p.Asp194=
NM_001372066.1:c.600C= (TFAP2A) MANE Select	NP_001358995.1:p.Asp200=
NM_001042425.3:c.582C= (TFAP2A)	NP_001035890.1:p.Asp194=