Canonical Allele Identifier: CA362701294

Gene: TFAP2A TFAP2A-AS2

Linked Data

• MyVariant Identifiers: chr6:g.10404806T>A (hg19) ; chr6:g.10404573T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404573T>A , CM000668.2:g.10404573T>A	GRCh38
NC_000006.11:g.10404806T>A , CM000668.1:g.10404806T>A	GRCh37
NC_000006.10:g.10512792T>A	NCBI36
NG_016151.1:g.19992A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.681A>T (TFAP2A)	ENSP00000368928.3:p.Glu227Asp
ENST00000379613.10:c.705A>T (TFAP2A) MANE Select	ENSP00000368933.5:p.Glu235Asp
ENST00000482890.6:c.705A>T (TFAP2A)	ENSP00000418541.2:p.Glu235Asp
ENST00000488193.7:c.*196A>T (TFAP2A)	ENSP00000419823.3:n.*196A>T
ENST00000498450.3:c.270A>T (TFAP2A)	ENSP00000419961.3:p.Glu90Asp
ENST00000319516.8:c.687A>T (TFAP2A)	ENSP00000316516.4:p.Glu229Asp
ENST00000379608.7:c.681A>T (TFAP2A)	ENSP00000368928.3:p.Glu227Asp
ENST00000379613.7:c.705A>T (TFAP2A)	ENSP00000368933.3:p.Glu235Asp
ENST00000461628.5:c.22A>T (TFAP2A)
ENST00000466073.5:c.699A>T (TFAP2A)	ENSP00000417495.1:p.Glu233Asp
ENST00000475264.5:c.413A>T (TFAP2A)
ENST00000478375.5:n.699A>T (TFAP2A)
ENST00000482890.5:c.699A>T (TFAP2A)	ENSP00000418541.1:p.Glu233Asp
ENST00000488193.5:c.*196A>T (TFAP2A)	ENSP00000419823.1:n.*196A>T
ENST00000489805.5:c.*196A>T (TFAP2A)	ENSP00000420568.1:n.*196A>T
ENST00000497266.5:n.670A>T (TFAP2A)
ENST00000498450.1:c.270A>T (TFAP2A)	ENSP00000419961.1:p.Glu90Asp
NM_001032280.2:c.681A>T (TFAP2A)	NP_001027451.1:p.Glu227Asp
NM_001042425.1:c.687A>T (TFAP2A)	NP_001035890.1:p.Glu229Asp
NM_003220.2:c.699A>T (TFAP2A)	NP_003211.1:p.Glu233Asp
XM_006715175.2:c.834A>T (TFAP2A)	XP_006715238.1:p.Glu278Asp
XM_011514833.1:c.549A>T (TFAP2A)	XP_011513135.1:p.Glu183Asp
NR_145448.1:n.72T>A (TFAP2A-AS2)
XM_011514833.2:c.549A>T (TFAP2A)	XP_011513135.1:p.Glu183Asp
XM_017011232.1:c.945A>T (TFAP2A)	XP_016866721.1:p.Glu315Asp
NM_003220.3:c.699A>T (TFAP2A)	NP_003211.1:p.Glu233Asp
NM_001032280.3:c.681A>T (TFAP2A)	NP_001027451.1:p.Glu227Asp
NM_001042425.2:c.687A>T (TFAP2A)	NP_001035890.1:p.Glu229Asp
NM_001372066.1:c.705A>T (TFAP2A) MANE Select	NP_001358995.1:p.Glu235Asp
NM_001042425.3:c.687A>T (TFAP2A)	NP_001035890.1:p.Glu229Asp