Canonical Allele Identifier: CA1609976767
Gene: TFAP2A HGNC NCBI
TFAP2A-AS2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10404615C= , CM000668.2:g.10404615C= GRCh38
NC_000006.11:g.10404848C= , CM000668.1:g.10404848C= GRCh37
NC_000006.10:g.10512834C= NCBI36
NG_016151.1:g.19950G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000379608.9:c.639G= (TFAP2A) ENSP00000368928.3:p.Ser213=
ENST00000379613.10:c.663G= (TFAP2A) MANE Select ENSP00000368933.5:p.Ser221=
ENST00000482890.6:c.663G= (TFAP2A) ENSP00000418541.2:p.Ser221=
ENST00000488193.7:c.*154G= (TFAP2A) ENSP00000419823.3:n.*154G=
ENST00000498450.3:c.228G= (TFAP2A) ENSP00000419961.3:p.Ser76=
ENST00000319516.8:c.645G= (TFAP2A) ENSP00000316516.4:p.Ser215=
ENST00000379608.7:c.639G= (TFAP2A) ENSP00000368928.3:p.Ser213=
ENST00000379613.7:c.663G= (TFAP2A) ENSP00000368933.3:p.Ser221=
ENST00000466073.5:c.657G= (TFAP2A) ENSP00000417495.1:p.Ser219=
ENST00000475264.5:c.371G= (TFAP2A)
ENST00000478375.5:n.657G= (TFAP2A)
ENST00000482890.5:c.657G= (TFAP2A) ENSP00000418541.1:p.Ser219=
ENST00000488193.5:c.*154G= (TFAP2A) ENSP00000419823.1:n.*154G=
ENST00000489805.5:c.*154G= (TFAP2A) ENSP00000420568.1:n.*154G=
ENST00000497266.5:n.628G= (TFAP2A)
ENST00000498450.1:c.228G= (TFAP2A) ENSP00000419961.1:p.Ser76=
NM_001032280.2:c.639G= (TFAP2A) NP_001027451.1:p.Ser213=
NM_001042425.1:c.645G= (TFAP2A) NP_001035890.1:p.Ser215=
NM_003220.2:c.657G= (TFAP2A) NP_003211.1:p.Ser219=
XM_006715175.2:c.792G= (TFAP2A) XP_006715238.1:p.Ser264=
XM_011514833.1:c.507G= (TFAP2A) XP_011513135.1:p.Ser169=
NR_145448.1:n.114C= (TFAP2A-AS2)
XM_011514833.2:c.507G= (TFAP2A) XP_011513135.1:p.Ser169=
XM_017011232.1:c.903G= (TFAP2A) XP_016866721.1:p.Ser301=
NM_003220.3:c.657G= (TFAP2A) NP_003211.1:p.Ser219=
NM_001032280.3:c.639G= (TFAP2A) NP_001027451.1:p.Ser213=
NM_001042425.2:c.645G= (TFAP2A) NP_001035890.1:p.Ser215=
NM_001372066.1:c.663G= (TFAP2A) MANE Select NP_001358995.1:p.Ser221=
NM_001042425.3:c.645G= (TFAP2A) NP_001035890.1:p.Ser215=