Canonical Allele Identifier: CA362701571

Gene: TFAP2A TFAP2A-AS2

Linked Data

• MyVariant Identifiers: chr6:g.10404874A>T (hg19) ; chr6:g.10404641A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404641A>T , CM000668.2:g.10404641A>T	GRCh38
NC_000006.11:g.10404874A>T , CM000668.1:g.10404874A>T	GRCh37
NC_000006.10:g.10512860A>T	NCBI36
NG_016151.1:g.19924T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.613T>A (TFAP2A)	ENSP00000368928.3:p.Phe205Ile
ENST00000379613.10:c.637T>A (TFAP2A) MANE Select	ENSP00000368933.5:p.Phe213Ile
ENST00000482890.6:c.637T>A (TFAP2A)	ENSP00000418541.2:p.Phe213Ile
ENST00000488193.7:c.*128T>A (TFAP2A)	ENSP00000419823.3:n.*128T>A
ENST00000498450.3:c.202T>A (TFAP2A)	ENSP00000419961.3:p.Phe68Ile
ENST00000319516.8:c.619T>A (TFAP2A)	ENSP00000316516.4:p.Phe207Ile
ENST00000379608.7:c.613T>A (TFAP2A)	ENSP00000368928.3:p.Phe205Ile
ENST00000379613.7:c.637T>A (TFAP2A)	ENSP00000368933.3:p.Phe213Ile
ENST00000466073.5:c.631T>A (TFAP2A)	ENSP00000417495.1:p.Phe211Ile
ENST00000475264.5:c.345T>A (TFAP2A)
ENST00000478375.5:n.631T>A (TFAP2A)
ENST00000482890.5:c.631T>A (TFAP2A)	ENSP00000418541.1:p.Phe211Ile
ENST00000488193.5:c.*128T>A (TFAP2A)	ENSP00000419823.1:n.*128T>A
ENST00000489805.5:c.*128T>A (TFAP2A)	ENSP00000420568.1:n.*128T>A
ENST00000490875.5:n.873T>A (TFAP2A)
ENST00000497266.5:n.602T>A (TFAP2A)
ENST00000498450.1:c.202T>A (TFAP2A)	ENSP00000419961.1:p.Phe68Ile
NM_001032280.2:c.613T>A (TFAP2A)	NP_001027451.1:p.Phe205Ile
NM_001042425.1:c.619T>A (TFAP2A)	NP_001035890.1:p.Phe207Ile
NM_003220.2:c.631T>A (TFAP2A)	NP_003211.1:p.Phe211Ile
XM_006715175.2:c.766T>A (TFAP2A)	XP_006715238.1:p.Phe256Ile
XM_011514833.1:c.481T>A (TFAP2A)	XP_011513135.1:p.Phe161Ile
NR_145448.1:n.140A>T (TFAP2A-AS2)
XM_011514833.2:c.481T>A (TFAP2A)	XP_011513135.1:p.Phe161Ile
XM_017011232.1:c.877T>A (TFAP2A)	XP_016866721.1:p.Phe293Ile
NM_003220.3:c.631T>A (TFAP2A)	NP_003211.1:p.Phe211Ile
NM_001032280.3:c.613T>A (TFAP2A)	NP_001027451.1:p.Phe205Ile
NM_001042425.2:c.619T>A (TFAP2A)	NP_001035890.1:p.Phe207Ile
NM_001372066.1:c.637T>A (TFAP2A) MANE Select	NP_001358995.1:p.Phe213Ile
NM_001042425.3:c.619T>A (TFAP2A)	NP_001035890.1:p.Phe207Ile