Canonical Allele Identifier: CA362701221
Gene: TFAP2A HGNC NCBI
TFAP2A-AS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10404551G>A , CM000668.2:g.10404551G>A GRCh38
NC_000006.11:g.10404784G>A , CM000668.1:g.10404784G>A GRCh37
NC_000006.10:g.10512770G>A NCBI36
NG_016151.1:g.20014C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379608.9:c.703C>T (TFAP2A) ENSP00000368928.3:p.Pro235Ser
ENST00000379613.10:c.727C>T (TFAP2A) MANE Select ENSP00000368933.5:p.Pro243Ser
ENST00000482890.6:c.727C>T (TFAP2A) ENSP00000418541.2:p.Pro243Ser
ENST00000488193.7:c.*218C>T (TFAP2A) ENSP00000419823.3:n.*218C>T
ENST00000498450.3:c.292C>T (TFAP2A) ENSP00000419961.3:p.Pro98Ser
ENST00000319516.8:c.709C>T (TFAP2A) ENSP00000316516.4:p.Pro237Ser
ENST00000379608.7:c.703C>T (TFAP2A) ENSP00000368928.3:p.Pro235Ser
ENST00000379613.7:c.727C>T (TFAP2A) ENSP00000368933.3:p.Pro243Ser
ENST00000461628.5:c.44C>T (TFAP2A)
ENST00000466073.5:c.721C>T (TFAP2A) ENSP00000417495.1:p.Pro241Ser
ENST00000475264.5:c.435C>T (TFAP2A)
ENST00000478375.5:n.721C>T (TFAP2A)
ENST00000482890.5:c.721C>T (TFAP2A) ENSP00000418541.1:p.Pro241Ser
ENST00000488193.5:c.*218C>T (TFAP2A) ENSP00000419823.1:n.*218C>T
ENST00000489805.5:c.*218C>T (TFAP2A) ENSP00000420568.1:n.*218C>T
ENST00000497266.5:n.692C>T (TFAP2A)
ENST00000498450.1:c.292C>T (TFAP2A) ENSP00000419961.1:p.Pro98Ser
NM_001032280.2:c.703C>T (TFAP2A) NP_001027451.1:p.Pro235Ser
NM_001042425.1:c.709C>T (TFAP2A) NP_001035890.1:p.Pro237Ser
NM_003220.2:c.721C>T (TFAP2A) NP_003211.1:p.Pro241Ser
XM_006715175.2:c.856C>T (TFAP2A) XP_006715238.1:p.Pro286Ser
XM_011514833.1:c.571C>T (TFAP2A) XP_011513135.1:p.Pro191Ser
NR_145448.1:n.50G>A (TFAP2A-AS2)
XM_011514833.2:c.571C>T (TFAP2A) XP_011513135.1:p.Pro191Ser
XM_017011232.1:c.967C>T (TFAP2A) XP_016866721.1:p.Pro323Ser
NM_003220.3:c.721C>T (TFAP2A) NP_003211.1:p.Pro241Ser
NM_001032280.3:c.703C>T (TFAP2A) NP_001027451.1:p.Pro235Ser
NM_001042425.2:c.709C>T (TFAP2A) NP_001035890.1:p.Pro237Ser
NM_001372066.1:c.727C>T (TFAP2A) MANE Select NP_001358995.1:p.Pro243Ser
NM_001042425.3:c.709C>T (TFAP2A) NP_001035890.1:p.Pro237Ser