Canonical Allele Identifier: CA448717873
Gene: TFAP2A HGNC NCBI
TFAP2A-AS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.10404932G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10404699G>T , CM000668.2:g.10404699G>T GRCh38
NC_000006.11:g.10404932G>T , CM000668.1:g.10404932G>T GRCh37
NC_000006.10:g.10512918G>T NCBI36
NG_016151.1:g.19866C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379608.9:c.555C>A (TFAP2A) ENSP00000368928.3:p.Ser185=
ENST00000379613.10:c.579C>A (TFAP2A) MANE Select ENSP00000368933.5:p.Ser193=
ENST00000482890.6:c.579C>A (TFAP2A) ENSP00000418541.2:p.Ser193=
ENST00000488193.7:c.*70C>A (TFAP2A) ENSP00000419823.3:n.*70C>A
ENST00000498450.3:c.144C>A (TFAP2A) ENSP00000419961.3:p.Ser48=
ENST00000319516.8:c.561C>A (TFAP2A) ENSP00000316516.4:p.Ser187=
ENST00000379608.7:c.555C>A (TFAP2A) ENSP00000368928.3:p.Ser185=
ENST00000379613.7:c.579C>A (TFAP2A) ENSP00000368933.3:p.Ser193=
ENST00000466073.5:c.573C>A (TFAP2A) ENSP00000417495.1:p.Ser191=
ENST00000473652.1:n.627C>A (TFAP2A)
ENST00000475264.5:c.287C>A (TFAP2A)
ENST00000478375.5:n.573C>A (TFAP2A)
ENST00000482890.5:c.573C>A (TFAP2A) ENSP00000418541.1:p.Ser191=
ENST00000488193.5:c.*70C>A (TFAP2A) ENSP00000419823.1:n.*70C>A
ENST00000489805.5:c.*70C>A (TFAP2A) ENSP00000420568.1:n.*70C>A
ENST00000490875.5:n.815C>A (TFAP2A)
ENST00000497266.5:n.544C>A (TFAP2A)
ENST00000498450.1:c.144C>A (TFAP2A) ENSP00000419961.1:p.Ser48=
NM_001032280.2:c.555C>A (TFAP2A) NP_001027451.1:p.Ser185=
NM_001042425.1:c.561C>A (TFAP2A) NP_001035890.1:p.Ser187=
NM_003220.2:c.573C>A (TFAP2A) NP_003211.1:p.Ser191=
XM_006715175.2:c.708C>A (TFAP2A) XP_006715238.1:p.Ser236=
XM_011514833.1:c.423C>A (TFAP2A) XP_011513135.1:p.Ser141=
NR_145448.1:n.198G>T (TFAP2A-AS2)
XM_011514833.2:c.423C>A (TFAP2A) XP_011513135.1:p.Ser141=
XM_017011232.1:c.819C>A (TFAP2A) XP_016866721.1:p.Ser273=
NM_003220.3:c.573C>A (TFAP2A) NP_003211.1:p.Ser191=
NM_001032280.3:c.555C>A (TFAP2A) NP_001027451.1:p.Ser185=
NM_001042425.2:c.561C>A (TFAP2A) NP_001035890.1:p.Ser187=
NM_001372066.1:c.579C>A (TFAP2A) MANE Select NP_001358995.1:p.Ser193=
NM_001042425.3:c.561C>A (TFAP2A) NP_001035890.1:p.Ser187=