Canonical Allele Identifier: CA362701263

Gene: TFAP2A TFAP2A-AS2

Linked Data

• MyVariant Identifiers: chr6:g.10404798C>T (hg19) ; chr6:g.10404565C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404565C>T , CM000668.2:g.10404565C>T	GRCh38
NC_000006.11:g.10404798C>T , CM000668.1:g.10404798C>T	GRCh37
NC_000006.10:g.10512784C>T	NCBI36
NG_016151.1:g.20000G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.689G>A (TFAP2A)	ENSP00000368928.3:p.Arg230Gln
ENST00000379613.10:c.713G>A (TFAP2A) MANE Select	ENSP00000368933.5:p.Arg238Gln
ENST00000482890.6:c.713G>A (TFAP2A)	ENSP00000418541.2:p.Arg238Gln
ENST00000488193.7:c.*204G>A (TFAP2A)	ENSP00000419823.3:n.*204G>A
ENST00000498450.3:c.278G>A (TFAP2A)	ENSP00000419961.3:p.Arg93Gln
ENST00000319516.8:c.695G>A (TFAP2A)	ENSP00000316516.4:p.Arg232Gln
ENST00000379608.7:c.689G>A (TFAP2A)	ENSP00000368928.3:p.Arg230Gln
ENST00000379613.7:c.713G>A (TFAP2A)	ENSP00000368933.3:p.Arg238Gln
ENST00000461628.5:c.30G>A (TFAP2A)
ENST00000466073.5:c.707G>A (TFAP2A)	ENSP00000417495.1:p.Arg236Gln
ENST00000475264.5:c.421G>A (TFAP2A)
ENST00000478375.5:n.707G>A (TFAP2A)
ENST00000482890.5:c.707G>A (TFAP2A)	ENSP00000418541.1:p.Arg236Gln
ENST00000488193.5:c.*204G>A (TFAP2A)	ENSP00000419823.1:n.*204G>A
ENST00000489805.5:c.*204G>A (TFAP2A)	ENSP00000420568.1:n.*204G>A
ENST00000497266.5:n.678G>A (TFAP2A)
ENST00000498450.1:c.278G>A (TFAP2A)	ENSP00000419961.1:p.Arg93Gln
NM_001032280.2:c.689G>A (TFAP2A)	NP_001027451.1:p.Arg230Gln
NM_001042425.1:c.695G>A (TFAP2A)	NP_001035890.1:p.Arg232Gln
NM_003220.2:c.707G>A (TFAP2A)	NP_003211.1:p.Arg236Gln
XM_006715175.2:c.842G>A (TFAP2A)	XP_006715238.1:p.Arg281Gln
XM_011514833.1:c.557G>A (TFAP2A)	XP_011513135.1:p.Arg186Gln
NR_145448.1:n.64C>T (TFAP2A-AS2)
XM_011514833.2:c.557G>A (TFAP2A)	XP_011513135.1:p.Arg186Gln
XM_017011232.1:c.953G>A (TFAP2A)	XP_016866721.1:p.Arg318Gln
NM_003220.3:c.707G>A (TFAP2A)	NP_003211.1:p.Arg236Gln
NM_001032280.3:c.689G>A (TFAP2A)	NP_001027451.1:p.Arg230Gln
NM_001042425.2:c.695G>A (TFAP2A)	NP_001035890.1:p.Arg232Gln
NM_001372066.1:c.713G>A (TFAP2A) MANE Select	NP_001358995.1:p.Arg238Gln
NM_001042425.3:c.695G>A (TFAP2A)	NP_001035890.1:p.Arg232Gln