Canonical Allele Identifier: CA362701709

Gene: TFAP2A TFAP2A-AS2

Linked Data

• MyVariant Identifiers: chr6:g.10404910T>A (hg19) ; chr6:g.10404677T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404677T>A , CM000668.2:g.10404677T>A	GRCh38
NC_000006.11:g.10404910T>A , CM000668.1:g.10404910T>A	GRCh37
NC_000006.10:g.10512896T>A	NCBI36
NG_016151.1:g.19888A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.577A>T (TFAP2A)	ENSP00000368928.3:p.Asn193Tyr
ENST00000379613.10:c.601A>T (TFAP2A) MANE Select	ENSP00000368933.5:p.Asn201Tyr
ENST00000482890.6:c.601A>T (TFAP2A)	ENSP00000418541.2:p.Asn201Tyr
ENST00000488193.7:c.*92A>T (TFAP2A)	ENSP00000419823.3:n.*92A>T
ENST00000498450.3:c.166A>T (TFAP2A)	ENSP00000419961.3:p.Asn56Tyr
ENST00000319516.8:c.583A>T (TFAP2A)	ENSP00000316516.4:p.Asn195Tyr
ENST00000379608.7:c.577A>T (TFAP2A)	ENSP00000368928.3:p.Asn193Tyr
ENST00000379613.7:c.601A>T (TFAP2A)	ENSP00000368933.3:p.Asn201Tyr
ENST00000466073.5:c.595A>T (TFAP2A)	ENSP00000417495.1:p.Asn199Tyr
ENST00000473652.1:n.649A>T (TFAP2A)
ENST00000475264.5:c.309A>T (TFAP2A)
ENST00000478375.5:n.595A>T (TFAP2A)
ENST00000482890.5:c.595A>T (TFAP2A)	ENSP00000418541.1:p.Asn199Tyr
ENST00000488193.5:c.*92A>T (TFAP2A)	ENSP00000419823.1:n.*92A>T
ENST00000489805.5:c.*92A>T (TFAP2A)	ENSP00000420568.1:n.*92A>T
ENST00000490875.5:n.837A>T (TFAP2A)
ENST00000497266.5:n.566A>T (TFAP2A)
ENST00000498450.1:c.166A>T (TFAP2A)	ENSP00000419961.1:p.Asn56Tyr
NM_001032280.2:c.577A>T (TFAP2A)	NP_001027451.1:p.Asn193Tyr
NM_001042425.1:c.583A>T (TFAP2A)	NP_001035890.1:p.Asn195Tyr
NM_003220.2:c.595A>T (TFAP2A)	NP_003211.1:p.Asn199Tyr
XM_006715175.2:c.730A>T (TFAP2A)	XP_006715238.1:p.Asn244Tyr
XM_011514833.1:c.445A>T (TFAP2A)	XP_011513135.1:p.Asn149Tyr
NR_145448.1:n.176T>A (TFAP2A-AS2)
XM_011514833.2:c.445A>T (TFAP2A)	XP_011513135.1:p.Asn149Tyr
XM_017011232.1:c.841A>T (TFAP2A)	XP_016866721.1:p.Asn281Tyr
NM_003220.3:c.595A>T (TFAP2A)	NP_003211.1:p.Asn199Tyr
NM_001032280.3:c.577A>T (TFAP2A)	NP_001027451.1:p.Asn193Tyr
NM_001042425.2:c.583A>T (TFAP2A)	NP_001035890.1:p.Asn195Tyr
NM_001372066.1:c.601A>T (TFAP2A) MANE Select	NP_001358995.1:p.Asn201Tyr
NM_001042425.3:c.583A>T (TFAP2A)	NP_001035890.1:p.Asn195Tyr