Canonical Allele Identifier: CA362701719
Gene: TFAP2A HGNC NCBI
TFAP2A-AS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10404679T>A , CM000668.2:g.10404679T>A GRCh38
NC_000006.11:g.10404912T>A , CM000668.1:g.10404912T>A GRCh37
NC_000006.10:g.10512898T>A NCBI36
NG_016151.1:g.19886A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000379608.9:c.575A>T (TFAP2A) ENSP00000368928.3:p.Asp192Val
ENST00000379613.10:c.599A>T (TFAP2A) MANE Select ENSP00000368933.5:p.Asp200Val
ENST00000482890.6:c.599A>T (TFAP2A) ENSP00000418541.2:p.Asp200Val
ENST00000488193.7:c.*90A>T (TFAP2A) ENSP00000419823.3:n.*90A>T
ENST00000498450.3:c.164A>T (TFAP2A) ENSP00000419961.3:p.Asp55Val
ENST00000319516.8:c.581A>T (TFAP2A) ENSP00000316516.4:p.Asp194Val
ENST00000379608.7:c.575A>T (TFAP2A) ENSP00000368928.3:p.Asp192Val
ENST00000379613.7:c.599A>T (TFAP2A) ENSP00000368933.3:p.Asp200Val
ENST00000466073.5:c.593A>T (TFAP2A) ENSP00000417495.1:p.Asp198Val
ENST00000473652.1:n.647A>T (TFAP2A)
ENST00000475264.5:c.307A>T (TFAP2A)
ENST00000478375.5:n.593A>T (TFAP2A)
ENST00000482890.5:c.593A>T (TFAP2A) ENSP00000418541.1:p.Asp198Val
ENST00000488193.5:c.*90A>T (TFAP2A) ENSP00000419823.1:n.*90A>T
ENST00000489805.5:c.*90A>T (TFAP2A) ENSP00000420568.1:n.*90A>T
ENST00000490875.5:n.835A>T (TFAP2A)
ENST00000497266.5:n.564A>T (TFAP2A)
ENST00000498450.1:c.164A>T (TFAP2A) ENSP00000419961.1:p.Asp55Val
NM_001032280.2:c.575A>T (TFAP2A) NP_001027451.1:p.Asp192Val
NM_001042425.1:c.581A>T (TFAP2A) NP_001035890.1:p.Asp194Val
NM_003220.2:c.593A>T (TFAP2A) NP_003211.1:p.Asp198Val
XM_006715175.2:c.728A>T (TFAP2A) XP_006715238.1:p.Asp243Val
XM_011514833.1:c.443A>T (TFAP2A) XP_011513135.1:p.Asp148Val
NR_145448.1:n.178T>A (TFAP2A-AS2)
XM_011514833.2:c.443A>T (TFAP2A) XP_011513135.1:p.Asp148Val
XM_017011232.1:c.839A>T (TFAP2A) XP_016866721.1:p.Asp280Val
NM_003220.3:c.593A>T (TFAP2A) NP_003211.1:p.Asp198Val
NM_001032280.3:c.575A>T (TFAP2A) NP_001027451.1:p.Asp192Val
NM_001042425.2:c.581A>T (TFAP2A) NP_001035890.1:p.Asp194Val
NM_001372066.1:c.599A>T (TFAP2A) MANE Select NP_001358995.1:p.Asp200Val
NM_001042425.3:c.581A>T (TFAP2A) NP_001035890.1:p.Asp194Val