Canonical Allele Identifier: CA448717493
Gene: TFAP2A HGNC NCBI
TFAP2A-AS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.10404776A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10404543A>G , CM000668.2:g.10404543A>G GRCh38
NC_000006.11:g.10404776A>G , CM000668.1:g.10404776A>G GRCh37
NC_000006.10:g.10512762A>G NCBI36
NG_016151.1:g.20022T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379608.9:c.711T>C (TFAP2A) ENSP00000368928.3:p.Cys237=
ENST00000379613.10:c.735T>C (TFAP2A) MANE Select ENSP00000368933.5:p.Cys245=
ENST00000482890.6:c.735T>C (TFAP2A) ENSP00000418541.2:p.Cys245=
ENST00000488193.7:c.*226T>C (TFAP2A) ENSP00000419823.3:n.*226T>C
ENST00000498450.3:c.300T>C (TFAP2A) ENSP00000419961.3:p.Cys100=
ENST00000319516.8:c.717T>C (TFAP2A) ENSP00000316516.4:p.Cys239=
ENST00000379608.7:c.711T>C (TFAP2A) ENSP00000368928.3:p.Cys237=
ENST00000379613.7:c.735T>C (TFAP2A) ENSP00000368933.3:p.Cys245=
ENST00000461628.5:c.52T>C (TFAP2A)
ENST00000466073.5:c.729T>C (TFAP2A) ENSP00000417495.1:p.Cys243=
ENST00000475264.5:c.443T>C (TFAP2A)
ENST00000478375.5:n.729T>C (TFAP2A)
ENST00000482890.5:c.729T>C (TFAP2A) ENSP00000418541.1:p.Cys243=
ENST00000488193.5:c.*226T>C (TFAP2A) ENSP00000419823.1:n.*226T>C
ENST00000489805.5:c.*226T>C (TFAP2A) ENSP00000420568.1:n.*226T>C
ENST00000497266.5:n.700T>C (TFAP2A)
ENST00000498450.1:c.300T>C (TFAP2A) ENSP00000419961.1:p.Cys100=
NM_001032280.2:c.711T>C (TFAP2A) NP_001027451.1:p.Cys237=
NM_001042425.1:c.717T>C (TFAP2A) NP_001035890.1:p.Cys239=
NM_003220.2:c.729T>C (TFAP2A) NP_003211.1:p.Cys243=
XM_006715175.2:c.864T>C (TFAP2A) XP_006715238.1:p.Cys288=
XM_011514833.1:c.579T>C (TFAP2A) XP_011513135.1:p.Cys193=
NR_145448.1:n.42A>G (TFAP2A-AS2)
XM_011514833.2:c.579T>C (TFAP2A) XP_011513135.1:p.Cys193=
XM_017011232.1:c.975T>C (TFAP2A) XP_016866721.1:p.Cys325=
NM_003220.3:c.729T>C (TFAP2A) NP_003211.1:p.Cys243=
NM_001032280.3:c.711T>C (TFAP2A) NP_001027451.1:p.Cys237=
NM_001042425.2:c.717T>C (TFAP2A) NP_001035890.1:p.Cys239=
NM_001372066.1:c.735T>C (TFAP2A) MANE Select NP_001358995.1:p.Cys245=
NM_001042425.3:c.717T>C (TFAP2A) NP_001035890.1:p.Cys239=