Canonical Allele Identifier: CA448717703
Gene: TFAP2A HGNC NCBI
TFAP2A-AS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.10404866T>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10404633T>G , CM000668.2:g.10404633T>G GRCh38
NC_000006.11:g.10404866T>G , CM000668.1:g.10404866T>G GRCh37
NC_000006.10:g.10512852T>G NCBI36
NG_016151.1:g.19932A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379608.9:c.621A>C (TFAP2A) ENSP00000368928.3:p.Ser207=
ENST00000379613.10:c.645A>C (TFAP2A) MANE Select ENSP00000368933.5:p.Ser215=
ENST00000482890.6:c.645A>C (TFAP2A) ENSP00000418541.2:p.Ser215=
ENST00000488193.7:c.*136A>C (TFAP2A) ENSP00000419823.3:n.*136A>C
ENST00000498450.3:c.210A>C (TFAP2A) ENSP00000419961.3:p.Ser70=
ENST00000319516.8:c.627A>C (TFAP2A) ENSP00000316516.4:p.Ser209=
ENST00000379608.7:c.621A>C (TFAP2A) ENSP00000368928.3:p.Ser207=
ENST00000379613.7:c.645A>C (TFAP2A) ENSP00000368933.3:p.Ser215=
ENST00000466073.5:c.639A>C (TFAP2A) ENSP00000417495.1:p.Ser213=
ENST00000475264.5:c.353A>C (TFAP2A)
ENST00000478375.5:n.639A>C (TFAP2A)
ENST00000482890.5:c.639A>C (TFAP2A) ENSP00000418541.1:p.Ser213=
ENST00000488193.5:c.*136A>C (TFAP2A) ENSP00000419823.1:n.*136A>C
ENST00000489805.5:c.*136A>C (TFAP2A) ENSP00000420568.1:n.*136A>C
ENST00000490875.5:n.881A>C (TFAP2A)
ENST00000497266.5:n.610A>C (TFAP2A)
ENST00000498450.1:c.210A>C (TFAP2A) ENSP00000419961.1:p.Ser70=
NM_001032280.2:c.621A>C (TFAP2A) NP_001027451.1:p.Ser207=
NM_001042425.1:c.627A>C (TFAP2A) NP_001035890.1:p.Ser209=
NM_003220.2:c.639A>C (TFAP2A) NP_003211.1:p.Ser213=
XM_006715175.2:c.774A>C (TFAP2A) XP_006715238.1:p.Ser258=
XM_011514833.1:c.489A>C (TFAP2A) XP_011513135.1:p.Ser163=
NR_145448.1:n.132T>G (TFAP2A-AS2)
XM_011514833.2:c.489A>C (TFAP2A) XP_011513135.1:p.Ser163=
XM_017011232.1:c.885A>C (TFAP2A) XP_016866721.1:p.Ser295=
NM_003220.3:c.639A>C (TFAP2A) NP_003211.1:p.Ser213=
NM_001032280.3:c.621A>C (TFAP2A) NP_001027451.1:p.Ser207=
NM_001042425.2:c.627A>C (TFAP2A) NP_001035890.1:p.Ser209=
NM_001372066.1:c.645A>C (TFAP2A) MANE Select NP_001358995.1:p.Ser215=
NM_001042425.3:c.627A>C (TFAP2A) NP_001035890.1:p.Ser209=