Canonical Allele Identifier: CA362701930
Gene: TFAP2A HGNC NCBI
TFAP2A-AS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10404728G>C , CM000668.2:g.10404728G>C GRCh38
NC_000006.11:g.10404961G>C , CM000668.1:g.10404961G>C GRCh37
NC_000006.10:g.10512947G>C NCBI36
NG_016151.1:g.19837C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000379608.9:c.526C>G (TFAP2A) ENSP00000368928.3:p.Leu176Val
ENST00000379613.10:c.550C>G (TFAP2A) MANE Select ENSP00000368933.5:p.Leu184Val
ENST00000482890.6:c.550C>G (TFAP2A) ENSP00000418541.2:p.Leu184Val
ENST00000488193.7:c.*41C>G (TFAP2A) ENSP00000419823.3:n.*41C>G
ENST00000498450.3:c.115C>G (TFAP2A) ENSP00000419961.3:p.Leu39Val
ENST00000319516.8:c.532C>G (TFAP2A) ENSP00000316516.4:p.Leu178Val
ENST00000379608.7:c.526C>G (TFAP2A) ENSP00000368928.3:p.Leu176Val
ENST00000379613.7:c.550C>G (TFAP2A) ENSP00000368933.3:p.Leu184Val
ENST00000466073.5:c.544C>G (TFAP2A) ENSP00000417495.1:p.Leu182Val
ENST00000473652.1:n.598C>G (TFAP2A)
ENST00000475264.5:c.258C>G (TFAP2A)
ENST00000478375.5:n.544C>G (TFAP2A)
ENST00000482890.5:c.544C>G (TFAP2A) ENSP00000418541.1:p.Leu182Val
ENST00000488193.5:c.*41C>G (TFAP2A) ENSP00000419823.1:n.*41C>G
ENST00000489805.5:c.*41C>G (TFAP2A) ENSP00000420568.1:n.*41C>G
ENST00000490875.5:n.786C>G (TFAP2A)
ENST00000497266.5:n.515C>G (TFAP2A)
ENST00000498450.1:c.115C>G (TFAP2A) ENSP00000419961.1:p.Leu39Val
NM_001032280.2:c.526C>G (TFAP2A) NP_001027451.1:p.Leu176Val
NM_001042425.1:c.532C>G (TFAP2A) NP_001035890.1:p.Leu178Val
NM_003220.2:c.544C>G (TFAP2A) NP_003211.1:p.Leu182Val
XM_006715175.2:c.679C>G (TFAP2A) XP_006715238.1:p.Leu227Val
XM_011514833.1:c.394C>G (TFAP2A) XP_011513135.1:p.Leu132Val
NR_145448.1:n.227G>C (TFAP2A-AS2)
XM_011514833.2:c.394C>G (TFAP2A) XP_011513135.1:p.Leu132Val
XM_017011232.1:c.790C>G (TFAP2A) XP_016866721.1:p.Leu264Val
NM_003220.3:c.544C>G (TFAP2A) NP_003211.1:p.Leu182Val
NM_001032280.3:c.526C>G (TFAP2A) NP_001027451.1:p.Leu176Val
NM_001042425.2:c.532C>G (TFAP2A) NP_001035890.1:p.Leu178Val
NM_001372066.1:c.550C>G (TFAP2A) MANE Select NP_001358995.1:p.Leu184Val
NM_001042425.3:c.532C>G (TFAP2A) NP_001035890.1:p.Leu178Val