Canonical Allele Identifier: CA645560345

Gene: TFAP2A TFAP2A-AS2

Linked Data

• COSMIC: COSM6233290 ; COSM6233291 ; COSM6233292

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404565del , CM000668.2:g.10404565del	GRCh38
NC_000006.11:g.10404798del , CM000668.1:g.10404798del	GRCh37
NC_000006.10:g.10512784del	NCBI36
NG_016151.1:g.20001del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.690del (TFAP2A)	ENSP00000368928.3:p.Arg231GlyfsTer29
ENST00000379613.10:c.714del (TFAP2A) MANE Select	ENSP00000368933.5:p.Arg239GlyfsTer29
ENST00000482890.6:c.714del (TFAP2A)	ENSP00000418541.2:p.Arg239GlyfsTer29
ENST00000488193.7:c.*205del (TFAP2A)	ENSP00000419823.3:n.*205del
ENST00000498450.3:c.279del (TFAP2A)	ENSP00000419961.3:p.Arg94GlyfsTer29
ENST00000319516.8:c.696del (TFAP2A)	ENSP00000316516.4:p.Arg233GlyfsTer29
ENST00000379608.7:c.690del (TFAP2A)	ENSP00000368928.3:p.Arg231GlyfsTer29
ENST00000379613.7:c.714del (TFAP2A)	ENSP00000368933.3:p.Arg239GlyfsTer29
ENST00000461628.5:c.31del (TFAP2A)
ENST00000466073.5:c.708del (TFAP2A)	ENSP00000417495.1:p.Arg237GlyfsTer29
ENST00000475264.5:c.422del (TFAP2A)
ENST00000478375.5:n.708del (TFAP2A)
ENST00000482890.5:c.708del (TFAP2A)	ENSP00000418541.1:p.Arg237GlyfsTer29
ENST00000488193.5:c.*205del (TFAP2A)	ENSP00000419823.1:n.*205del
ENST00000489805.5:c.*205del (TFAP2A)	ENSP00000420568.1:n.*205del
ENST00000497266.5:n.679del (TFAP2A)
ENST00000498450.1:c.279del (TFAP2A)	ENSP00000419961.1:p.Arg94GlyfsTer29
NM_001032280.2:c.690del (TFAP2A)	NP_001027451.1:p.Arg231GlyfsTer29
NM_001042425.1:c.696del (TFAP2A)	NP_001035890.1:p.Arg233GlyfsTer29
NM_003220.2:c.708del (TFAP2A)	NP_003211.1:p.Arg237GlyfsTer29
XM_006715175.2:c.843del (TFAP2A)	XP_006715238.1:p.Arg282GlyfsTer29
XM_011514833.1:c.558del (TFAP2A)	XP_011513135.1:p.Arg187GlyfsTer29
NR_145448.1:n.64del (TFAP2A-AS2)
XM_011514833.2:c.558del (TFAP2A)	XP_011513135.1:p.Arg187GlyfsTer29
XM_017011232.1:c.954del (TFAP2A)	XP_016866721.1:p.Arg319GlyfsTer29
NM_003220.3:c.708del (TFAP2A)	NP_003211.1:p.Arg237GlyfsTer29
NM_001032280.3:c.690del (TFAP2A)	NP_001027451.1:p.Arg231GlyfsTer29
NM_001042425.2:c.696del (TFAP2A)	NP_001035890.1:p.Arg233GlyfsTer29
NM_001372066.1:c.714del (TFAP2A) MANE Select	NP_001358995.1:p.Arg239GlyfsTer29
NM_001042425.3:c.696del (TFAP2A)	NP_001035890.1:p.Arg233GlyfsTer29