Canonical Allele Identifier: CA362701243

Gene: TFAP2A TFAP2A-AS2

Linked Data

• MyVariant Identifiers: chr6:g.10404792A>T (hg19) ; chr6:g.10404559A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404559A>T , CM000668.2:g.10404559A>T	GRCh38
NC_000006.11:g.10404792A>T , CM000668.1:g.10404792A>T	GRCh37
NC_000006.10:g.10512778A>T	NCBI36
NG_016151.1:g.20006T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.695T>A (TFAP2A)	ENSP00000368928.3:p.Leu232His
ENST00000379613.10:c.719T>A (TFAP2A) MANE Select	ENSP00000368933.5:p.Leu240His
ENST00000482890.6:c.719T>A (TFAP2A)	ENSP00000418541.2:p.Leu240His
ENST00000488193.7:c.*210T>A (TFAP2A)	ENSP00000419823.3:n.*210T>A
ENST00000498450.3:c.284T>A (TFAP2A)	ENSP00000419961.3:p.Leu95His
ENST00000319516.8:c.701T>A (TFAP2A)	ENSP00000316516.4:p.Leu234His
ENST00000379608.7:c.695T>A (TFAP2A)	ENSP00000368928.3:p.Leu232His
ENST00000379613.7:c.719T>A (TFAP2A)	ENSP00000368933.3:p.Leu240His
ENST00000461628.5:c.36T>A (TFAP2A)
ENST00000466073.5:c.713T>A (TFAP2A)	ENSP00000417495.1:p.Leu238His
ENST00000475264.5:c.427T>A (TFAP2A)
ENST00000478375.5:n.713T>A (TFAP2A)
ENST00000482890.5:c.713T>A (TFAP2A)	ENSP00000418541.1:p.Leu238His
ENST00000488193.5:c.*210T>A (TFAP2A)	ENSP00000419823.1:n.*210T>A
ENST00000489805.5:c.*210T>A (TFAP2A)	ENSP00000420568.1:n.*210T>A
ENST00000497266.5:n.684T>A (TFAP2A)
ENST00000498450.1:c.284T>A (TFAP2A)	ENSP00000419961.1:p.Leu95His
NM_001032280.2:c.695T>A (TFAP2A)	NP_001027451.1:p.Leu232His
NM_001042425.1:c.701T>A (TFAP2A)	NP_001035890.1:p.Leu234His
NM_003220.2:c.713T>A (TFAP2A)	NP_003211.1:p.Leu238His
XM_006715175.2:c.848T>A (TFAP2A)	XP_006715238.1:p.Leu283His
XM_011514833.1:c.563T>A (TFAP2A)	XP_011513135.1:p.Leu188His
NR_145448.1:n.58A>T (TFAP2A-AS2)
XM_011514833.2:c.563T>A (TFAP2A)	XP_011513135.1:p.Leu188His
XM_017011232.1:c.959T>A (TFAP2A)	XP_016866721.1:p.Leu320His
NM_003220.3:c.713T>A (TFAP2A)	NP_003211.1:p.Leu238His
NM_001032280.3:c.695T>A (TFAP2A)	NP_001027451.1:p.Leu232His
NM_001042425.2:c.701T>A (TFAP2A)	NP_001035890.1:p.Leu234His
NM_001372066.1:c.719T>A (TFAP2A) MANE Select	NP_001358995.1:p.Leu240His
NM_001042425.3:c.701T>A (TFAP2A)	NP_001035890.1:p.Leu234His