Canonical Allele Identifier: CA362701167
Gene: TFAP2A HGNC NCBI
TFAP2A-AS2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10404524C>G , CM000668.2:g.10404524C>G GRCh38
NC_000006.11:g.10404757C>G , CM000668.1:g.10404757C>G GRCh37
NC_000006.10:g.10512743C>G NCBI36
NG_016151.1:g.20041G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000379608.9:c.730G>C (TFAP2A) ENSP00000368928.3:p.Gly244Arg
ENST00000379613.10:c.754G>C (TFAP2A) MANE Select ENSP00000368933.5:p.Gly252Arg
ENST00000482890.6:c.754G>C (TFAP2A) ENSP00000418541.2:p.Gly252Arg
ENST00000488193.7:c.*245G>C (TFAP2A) ENSP00000419823.3:n.*245G>C
ENST00000498450.3:c.319G>C (TFAP2A) ENSP00000419961.3:p.Gly107Arg
ENST00000319516.8:c.736G>C (TFAP2A) ENSP00000316516.4:p.Gly246Arg
ENST00000379608.7:c.730G>C (TFAP2A) ENSP00000368928.3:p.Gly244Arg
ENST00000379613.7:c.754G>C (TFAP2A) ENSP00000368933.3:p.Gly252Arg
ENST00000461628.5:c.71G>C (TFAP2A)
ENST00000466073.5:c.748G>C (TFAP2A) ENSP00000417495.1:p.Gly250Arg
ENST00000475264.5:c.462G>C (TFAP2A)
ENST00000478375.5:n.748G>C (TFAP2A)
ENST00000482890.5:c.748G>C (TFAP2A) ENSP00000418541.1:p.Gly250Arg
ENST00000488193.5:c.*245G>C (TFAP2A) ENSP00000419823.1:n.*245G>C
ENST00000489805.5:c.*245G>C (TFAP2A) ENSP00000420568.1:n.*245G>C
ENST00000497266.5:n.719G>C (TFAP2A)
ENST00000498450.1:c.319G>C (TFAP2A) ENSP00000419961.1:p.Gly107Arg
NM_001032280.2:c.730G>C (TFAP2A) NP_001027451.1:p.Gly244Arg
NM_001042425.1:c.736G>C (TFAP2A) NP_001035890.1:p.Gly246Arg
NM_003220.2:c.748G>C (TFAP2A) NP_003211.1:p.Gly250Arg
XM_006715175.2:c.883G>C (TFAP2A) XP_006715238.1:p.Gly295Arg
XM_011514833.1:c.598G>C (TFAP2A) XP_011513135.1:p.Gly200Arg
NR_145448.1:n.23C>G (TFAP2A-AS2)
XM_011514833.2:c.598G>C (TFAP2A) XP_011513135.1:p.Gly200Arg
XM_017011232.1:c.994G>C (TFAP2A) XP_016866721.1:p.Gly332Arg
NM_003220.3:c.748G>C (TFAP2A) NP_003211.1:p.Gly250Arg
NM_001032280.3:c.730G>C (TFAP2A) NP_001027451.1:p.Gly244Arg
NM_001042425.2:c.736G>C (TFAP2A) NP_001035890.1:p.Gly246Arg
NM_001372066.1:c.754G>C (TFAP2A) MANE Select NP_001358995.1:p.Gly252Arg
NM_001042425.3:c.736G>C (TFAP2A) NP_001035890.1:p.Gly246Arg