Canonical Allele Identifier: CA362701483

Gene: TFAP2A TFAP2A-AS2

Linked Data

• MyVariant Identifiers: chr6:g.10404852A>T (hg19) ; chr6:g.10404619A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404619A>T , CM000668.2:g.10404619A>T	GRCh38
NC_000006.11:g.10404852A>T , CM000668.1:g.10404852A>T	GRCh37
NC_000006.10:g.10512838A>T	NCBI36
NG_016151.1:g.19946T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.635T>A (TFAP2A)	ENSP00000368928.3:p.Leu212His
ENST00000379613.10:c.659T>A (TFAP2A) MANE Select	ENSP00000368933.5:p.Leu220His
ENST00000482890.6:c.659T>A (TFAP2A)	ENSP00000418541.2:p.Leu220His
ENST00000488193.7:c.*150T>A (TFAP2A)	ENSP00000419823.3:n.*150T>A
ENST00000498450.3:c.224T>A (TFAP2A)	ENSP00000419961.3:p.Leu75His
ENST00000319516.8:c.641T>A (TFAP2A)	ENSP00000316516.4:p.Leu214His
ENST00000379608.7:c.635T>A (TFAP2A)	ENSP00000368928.3:p.Leu212His
ENST00000379613.7:c.659T>A (TFAP2A)	ENSP00000368933.3:p.Leu220His
ENST00000466073.5:c.653T>A (TFAP2A)	ENSP00000417495.1:p.Leu218His
ENST00000475264.5:c.367T>A (TFAP2A)
ENST00000478375.5:n.653T>A (TFAP2A)
ENST00000482890.5:c.653T>A (TFAP2A)	ENSP00000418541.1:p.Leu218His
ENST00000488193.5:c.*150T>A (TFAP2A)	ENSP00000419823.1:n.*150T>A
ENST00000489805.5:c.*150T>A (TFAP2A)	ENSP00000420568.1:n.*150T>A
ENST00000497266.5:n.624T>A (TFAP2A)
ENST00000498450.1:c.224T>A (TFAP2A)	ENSP00000419961.1:p.Leu75His
NM_001032280.2:c.635T>A (TFAP2A)	NP_001027451.1:p.Leu212His
NM_001042425.1:c.641T>A (TFAP2A)	NP_001035890.1:p.Leu214His
NM_003220.2:c.653T>A (TFAP2A)	NP_003211.1:p.Leu218His
XM_006715175.2:c.788T>A (TFAP2A)	XP_006715238.1:p.Leu263His
XM_011514833.1:c.503T>A (TFAP2A)	XP_011513135.1:p.Leu168His
NR_145448.1:n.118A>T (TFAP2A-AS2)
XM_011514833.2:c.503T>A (TFAP2A)	XP_011513135.1:p.Leu168His
XM_017011232.1:c.899T>A (TFAP2A)	XP_016866721.1:p.Leu300His
NM_003220.3:c.653T>A (TFAP2A)	NP_003211.1:p.Leu218His
NM_001032280.3:c.635T>A (TFAP2A)	NP_001027451.1:p.Leu212His
NM_001042425.2:c.641T>A (TFAP2A)	NP_001035890.1:p.Leu214His
NM_001372066.1:c.659T>A (TFAP2A) MANE Select	NP_001358995.1:p.Leu220His
NM_001042425.3:c.641T>A (TFAP2A)	NP_001035890.1:p.Leu214His