Canonical Allele Identifier: CA362701823

Gene: TFAP2A TFAP2A-AS2

Linked Data

• MyVariant Identifiers: chr6:g.10404936A>T (hg19) ; chr6:g.10404703A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404703A>T , CM000668.2:g.10404703A>T	GRCh38
NC_000006.11:g.10404936A>T , CM000668.1:g.10404936A>T	GRCh37
NC_000006.10:g.10512922A>T	NCBI36
NG_016151.1:g.19862T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.551T>A (TFAP2A)	ENSP00000368928.3:p.Val184Asp
ENST00000379613.10:c.575T>A (TFAP2A) MANE Select	ENSP00000368933.5:p.Val192Asp
ENST00000482890.6:c.575T>A (TFAP2A)	ENSP00000418541.2:p.Val192Asp
ENST00000488193.7:c.*66T>A (TFAP2A)	ENSP00000419823.3:n.*66T>A
ENST00000498450.3:c.140T>A (TFAP2A)	ENSP00000419961.3:p.Val47Asp
ENST00000319516.8:c.557T>A (TFAP2A)	ENSP00000316516.4:p.Val186Asp
ENST00000379608.7:c.551T>A (TFAP2A)	ENSP00000368928.3:p.Val184Asp
ENST00000379613.7:c.575T>A (TFAP2A)	ENSP00000368933.3:p.Val192Asp
ENST00000466073.5:c.569T>A (TFAP2A)	ENSP00000417495.1:p.Val190Asp
ENST00000473652.1:n.623T>A (TFAP2A)
ENST00000475264.5:c.283T>A (TFAP2A)
ENST00000478375.5:n.569T>A (TFAP2A)
ENST00000482890.5:c.569T>A (TFAP2A)	ENSP00000418541.1:p.Val190Asp
ENST00000488193.5:c.*66T>A (TFAP2A)	ENSP00000419823.1:n.*66T>A
ENST00000489805.5:c.*66T>A (TFAP2A)	ENSP00000420568.1:n.*66T>A
ENST00000490875.5:n.811T>A (TFAP2A)
ENST00000497266.5:n.540T>A (TFAP2A)
ENST00000498450.1:c.140T>A (TFAP2A)	ENSP00000419961.1:p.Val47Asp
NM_001032280.2:c.551T>A (TFAP2A)	NP_001027451.1:p.Val184Asp
NM_001042425.1:c.557T>A (TFAP2A)	NP_001035890.1:p.Val186Asp
NM_003220.2:c.569T>A (TFAP2A)	NP_003211.1:p.Val190Asp
XM_006715175.2:c.704T>A (TFAP2A)	XP_006715238.1:p.Val235Asp
XM_011514833.1:c.419T>A (TFAP2A)	XP_011513135.1:p.Val140Asp
NR_145448.1:n.202A>T (TFAP2A-AS2)
XM_011514833.2:c.419T>A (TFAP2A)	XP_011513135.1:p.Val140Asp
XM_017011232.1:c.815T>A (TFAP2A)	XP_016866721.1:p.Val272Asp
NM_003220.3:c.569T>A (TFAP2A)	NP_003211.1:p.Val190Asp
NM_001032280.3:c.551T>A (TFAP2A)	NP_001027451.1:p.Val184Asp
NM_001042425.2:c.557T>A (TFAP2A)	NP_001035890.1:p.Val186Asp
NM_001372066.1:c.575T>A (TFAP2A) MANE Select	NP_001358995.1:p.Val192Asp
NM_001042425.3:c.557T>A (TFAP2A)	NP_001035890.1:p.Val186Asp