Canonical Allele Identifier: CA362701706
Gene: TFAP2A HGNC NCBI
TFAP2A-AS2 HGNC NCBI

Linked Data

gnomAD v4: 6-10404676-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10404676T>C , CM000668.2:g.10404676T>C GRCh38
NC_000006.11:g.10404909T>C , CM000668.1:g.10404909T>C GRCh37
NC_000006.10:g.10512895T>C NCBI36
NG_016151.1:g.19889A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000379608.9:c.578A>G (TFAP2A) ENSP00000368928.3:p.Asn193Ser
ENST00000379613.10:c.602A>G (TFAP2A) MANE Select ENSP00000368933.5:p.Asn201Ser
ENST00000482890.6:c.602A>G (TFAP2A) ENSP00000418541.2:p.Asn201Ser
ENST00000488193.7:c.*93A>G (TFAP2A) ENSP00000419823.3:n.*93A>G
ENST00000498450.3:c.167A>G (TFAP2A) ENSP00000419961.3:p.Asn56Ser
ENST00000319516.8:c.584A>G (TFAP2A) ENSP00000316516.4:p.Asn195Ser
ENST00000379608.7:c.578A>G (TFAP2A) ENSP00000368928.3:p.Asn193Ser
ENST00000379613.7:c.602A>G (TFAP2A) ENSP00000368933.3:p.Asn201Ser
ENST00000466073.5:c.596A>G (TFAP2A) ENSP00000417495.1:p.Asn199Ser
ENST00000473652.1:n.650A>G (TFAP2A)
ENST00000475264.5:c.310A>G (TFAP2A)
ENST00000478375.5:n.596A>G (TFAP2A)
ENST00000482890.5:c.596A>G (TFAP2A) ENSP00000418541.1:p.Asn199Ser
ENST00000488193.5:c.*93A>G (TFAP2A) ENSP00000419823.1:n.*93A>G
ENST00000489805.5:c.*93A>G (TFAP2A) ENSP00000420568.1:n.*93A>G
ENST00000490875.5:n.838A>G (TFAP2A)
ENST00000497266.5:n.567A>G (TFAP2A)
ENST00000498450.1:c.167A>G (TFAP2A) ENSP00000419961.1:p.Asn56Ser
NM_001032280.2:c.578A>G (TFAP2A) NP_001027451.1:p.Asn193Ser
NM_001042425.1:c.584A>G (TFAP2A) NP_001035890.1:p.Asn195Ser
NM_003220.2:c.596A>G (TFAP2A) NP_003211.1:p.Asn199Ser
XM_006715175.2:c.731A>G (TFAP2A) XP_006715238.1:p.Asn244Ser
XM_011514833.1:c.446A>G (TFAP2A) XP_011513135.1:p.Asn149Ser
NR_145448.1:n.175T>C (TFAP2A-AS2)
XM_011514833.2:c.446A>G (TFAP2A) XP_011513135.1:p.Asn149Ser
XM_017011232.1:c.842A>G (TFAP2A) XP_016866721.1:p.Asn281Ser
NM_003220.3:c.596A>G (TFAP2A) NP_003211.1:p.Asn199Ser
NM_001032280.3:c.578A>G (TFAP2A) NP_001027451.1:p.Asn193Ser
NM_001042425.2:c.584A>G (TFAP2A) NP_001035890.1:p.Asn195Ser
NM_001372066.1:c.602A>G (TFAP2A) MANE Select NP_001358995.1:p.Asn201Ser
NM_001042425.3:c.584A>G (TFAP2A) NP_001035890.1:p.Asn195Ser