Canonical Allele Identifier: CA3631280
Gene: TFAP2A HGNC NCBI
TFAP2A-AS2 HGNC NCBI

Linked Data

dbSNP Id: rs772033707
gnomAD v2: 6-10404902-G-T
gnomAD v4: 6-10404669-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10404669G>T , CM000668.2:g.10404669G>T GRCh38
NC_000006.11:g.10404902G>T , CM000668.1:g.10404902G>T GRCh37
NC_000006.10:g.10512888G>T NCBI36
NG_016151.1:g.19896C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379608.9:c.585C>A (TFAP2A) ENSP00000368928.3:p.Phe195Leu
ENST00000379613.10:c.609C>A (TFAP2A) MANE Select ENSP00000368933.5:p.Phe203Leu
ENST00000482890.6:c.609C>A (TFAP2A) ENSP00000418541.2:p.Phe203Leu
ENST00000488193.7:c.*100C>A (TFAP2A) ENSP00000419823.3:n.*100C>A
ENST00000498450.3:c.174C>A (TFAP2A) ENSP00000419961.3:p.Phe58Leu
ENST00000319516.8:c.591C>A (TFAP2A) ENSP00000316516.4:p.Phe197Leu
ENST00000379608.7:c.585C>A (TFAP2A) ENSP00000368928.3:p.Phe195Leu
ENST00000379613.7:c.609C>A (TFAP2A) ENSP00000368933.3:p.Phe203Leu
ENST00000466073.5:c.603C>A (TFAP2A) ENSP00000417495.1:p.Phe201Leu
ENST00000473652.1:n.657C>A (TFAP2A)
ENST00000475264.5:c.317C>A (TFAP2A)
ENST00000478375.5:n.603C>A (TFAP2A)
ENST00000482890.5:c.603C>A (TFAP2A) ENSP00000418541.1:p.Phe201Leu
ENST00000488193.5:c.*100C>A (TFAP2A) ENSP00000419823.1:n.*100C>A
ENST00000489805.5:c.*100C>A (TFAP2A) ENSP00000420568.1:n.*100C>A
ENST00000490875.5:n.845C>A (TFAP2A)
ENST00000497266.5:n.574C>A (TFAP2A)
ENST00000498450.1:c.174C>A (TFAP2A) ENSP00000419961.1:p.Phe58Leu
NM_001032280.2:c.585C>A (TFAP2A) NP_001027451.1:p.Phe195Leu
NM_001042425.1:c.591C>A (TFAP2A) NP_001035890.1:p.Phe197Leu
NM_003220.2:c.603C>A (TFAP2A) NP_003211.1:p.Phe201Leu
XM_006715175.2:c.738C>A (TFAP2A) XP_006715238.1:p.Phe246Leu
XM_011514833.1:c.453C>A (TFAP2A) XP_011513135.1:p.Phe151Leu
NR_145448.1:n.168G>T (TFAP2A-AS2)
XM_011514833.2:c.453C>A (TFAP2A) XP_011513135.1:p.Phe151Leu
XM_017011232.1:c.849C>A (TFAP2A) XP_016866721.1:p.Phe283Leu
NM_003220.3:c.603C>A (TFAP2A) NP_003211.1:p.Phe201Leu
NM_001032280.3:c.585C>A (TFAP2A) NP_001027451.1:p.Phe195Leu
NM_001042425.2:c.591C>A (TFAP2A) NP_001035890.1:p.Phe197Leu
NM_001372066.1:c.609C>A (TFAP2A) MANE Select NP_001358995.1:p.Phe203Leu
NM_001042425.3:c.591C>A (TFAP2A) NP_001035890.1:p.Phe197Leu