Canonical Allele Identifier: CA362701897
Gene: TFAP2A HGNC NCBI
TFAP2A-AS2 HGNC NCBI

Linked Data

dbSNP Id: rs201296512

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10404716T>G , CM000668.2:g.10404716T>G GRCh38
NC_000006.11:g.10404949T>G , CM000668.1:g.10404949T>G GRCh37
NC_000006.10:g.10512935T>G NCBI36
NG_016151.1:g.19849A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379608.9:c.538A>C (TFAP2A) ENSP00000368928.3:p.Asn180His
ENST00000379613.10:c.562A>C (TFAP2A) MANE Select ENSP00000368933.5:p.Asn188His
ENST00000482890.6:c.562A>C (TFAP2A) ENSP00000418541.2:p.Asn188His
ENST00000488193.7:c.*53A>C (TFAP2A) ENSP00000419823.3:n.*53A>C
ENST00000498450.3:c.127A>C (TFAP2A) ENSP00000419961.3:p.Asn43His
ENST00000319516.8:c.544A>C (TFAP2A) ENSP00000316516.4:p.Asn182His
ENST00000379608.7:c.538A>C (TFAP2A) ENSP00000368928.3:p.Asn180His
ENST00000379613.7:c.562A>C (TFAP2A) ENSP00000368933.3:p.Asn188His
ENST00000466073.5:c.556A>C (TFAP2A) ENSP00000417495.1:p.Asn186His
ENST00000473652.1:n.610A>C (TFAP2A)
ENST00000475264.5:c.270A>C (TFAP2A)
ENST00000478375.5:n.556A>C (TFAP2A)
ENST00000482890.5:c.556A>C (TFAP2A) ENSP00000418541.1:p.Asn186His
ENST00000488193.5:c.*53A>C (TFAP2A) ENSP00000419823.1:n.*53A>C
ENST00000489805.5:c.*53A>C (TFAP2A) ENSP00000420568.1:n.*53A>C
ENST00000490875.5:n.798A>C (TFAP2A)
ENST00000497266.5:n.527A>C (TFAP2A)
ENST00000498450.1:c.127A>C (TFAP2A) ENSP00000419961.1:p.Asn43His
NM_001032280.2:c.538A>C (TFAP2A) NP_001027451.1:p.Asn180His
NM_001042425.1:c.544A>C (TFAP2A) NP_001035890.1:p.Asn182His
NM_003220.2:c.556A>C (TFAP2A) NP_003211.1:p.Asn186His
XM_006715175.2:c.691A>C (TFAP2A) XP_006715238.1:p.Asn231His
XM_011514833.1:c.406A>C (TFAP2A) XP_011513135.1:p.Asn136His
NR_145448.1:n.215T>G (TFAP2A-AS2)
XM_011514833.2:c.406A>C (TFAP2A) XP_011513135.1:p.Asn136His
XM_017011232.1:c.802A>C (TFAP2A) XP_016866721.1:p.Asn268His
NM_003220.3:c.556A>C (TFAP2A) NP_003211.1:p.Asn186His
NM_001032280.3:c.538A>C (TFAP2A) NP_001027451.1:p.Asn180His
NM_001042425.2:c.544A>C (TFAP2A) NP_001035890.1:p.Asn182His
NM_001372066.1:c.562A>C (TFAP2A) MANE Select NP_001358995.1:p.Asn188His
NM_001042425.3:c.544A>C (TFAP2A) NP_001035890.1:p.Asn182His