Canonical Allele Identifier: CA362701924

Gene: TFAP2A TFAP2A-AS2

Linked Data

• MyVariant Identifiers: chr6:g.10404958A>G (hg19) ; chr6:g.10404725A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404725A>G , CM000668.2:g.10404725A>G	GRCh38
NC_000006.11:g.10404958A>G , CM000668.1:g.10404958A>G	GRCh37
NC_000006.10:g.10512944A>G	NCBI36
NG_016151.1:g.19840T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.529T>C (TFAP2A)	ENSP00000368928.3:p.Ser177Pro
ENST00000379613.10:c.553T>C (TFAP2A) MANE Select	ENSP00000368933.5:p.Ser185Pro
ENST00000482890.6:c.553T>C (TFAP2A)	ENSP00000418541.2:p.Ser185Pro
ENST00000488193.7:c.*44T>C (TFAP2A)	ENSP00000419823.3:n.*44T>C
ENST00000498450.3:c.118T>C (TFAP2A)	ENSP00000419961.3:p.Ser40Pro
ENST00000319516.8:c.535T>C (TFAP2A)	ENSP00000316516.4:p.Ser179Pro
ENST00000379608.7:c.529T>C (TFAP2A)	ENSP00000368928.3:p.Ser177Pro
ENST00000379613.7:c.553T>C (TFAP2A)	ENSP00000368933.3:p.Ser185Pro
ENST00000466073.5:c.547T>C (TFAP2A)	ENSP00000417495.1:p.Ser183Pro
ENST00000473652.1:n.601T>C (TFAP2A)
ENST00000475264.5:c.261T>C (TFAP2A)
ENST00000478375.5:n.547T>C (TFAP2A)
ENST00000482890.5:c.547T>C (TFAP2A)	ENSP00000418541.1:p.Ser183Pro
ENST00000488193.5:c.*44T>C (TFAP2A)	ENSP00000419823.1:n.*44T>C
ENST00000489805.5:c.*44T>C (TFAP2A)	ENSP00000420568.1:n.*44T>C
ENST00000490875.5:n.789T>C (TFAP2A)
ENST00000497266.5:n.518T>C (TFAP2A)
ENST00000498450.1:c.118T>C (TFAP2A)	ENSP00000419961.1:p.Ser40Pro
NM_001032280.2:c.529T>C (TFAP2A)	NP_001027451.1:p.Ser177Pro
NM_001042425.1:c.535T>C (TFAP2A)	NP_001035890.1:p.Ser179Pro
NM_003220.2:c.547T>C (TFAP2A)	NP_003211.1:p.Ser183Pro
XM_006715175.2:c.682T>C (TFAP2A)	XP_006715238.1:p.Ser228Pro
XM_011514833.1:c.397T>C (TFAP2A)	XP_011513135.1:p.Ser133Pro
NR_145448.1:n.224A>G (TFAP2A-AS2)
XM_011514833.2:c.397T>C (TFAP2A)	XP_011513135.1:p.Ser133Pro
XM_017011232.1:c.793T>C (TFAP2A)	XP_016866721.1:p.Ser265Pro
NM_003220.3:c.547T>C (TFAP2A)	NP_003211.1:p.Ser183Pro
NM_001032280.3:c.529T>C (TFAP2A)	NP_001027451.1:p.Ser177Pro
NM_001042425.2:c.535T>C (TFAP2A)	NP_001035890.1:p.Ser179Pro
NM_001372066.1:c.553T>C (TFAP2A) MANE Select	NP_001358995.1:p.Ser185Pro
NM_001042425.3:c.535T>C (TFAP2A)	NP_001035890.1:p.Ser179Pro