Canonical Allele Identifier: CA448717878
Gene: TFAP2A HGNC NCBI
TFAP2A-AS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.10404935G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10404702G>C , CM000668.2:g.10404702G>C GRCh38
NC_000006.11:g.10404935G>C , CM000668.1:g.10404935G>C GRCh37
NC_000006.10:g.10512921G>C NCBI36
NG_016151.1:g.19863C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000379608.9:c.552C>G (TFAP2A) ENSP00000368928.3:p.Val184=
ENST00000379613.10:c.576C>G (TFAP2A) MANE Select ENSP00000368933.5:p.Val192=
ENST00000482890.6:c.576C>G (TFAP2A) ENSP00000418541.2:p.Val192=
ENST00000488193.7:c.*67C>G (TFAP2A) ENSP00000419823.3:n.*67C>G
ENST00000498450.3:c.141C>G (TFAP2A) ENSP00000419961.3:p.Val47=
ENST00000319516.8:c.558C>G (TFAP2A) ENSP00000316516.4:p.Val186=
ENST00000379608.7:c.552C>G (TFAP2A) ENSP00000368928.3:p.Val184=
ENST00000379613.7:c.576C>G (TFAP2A) ENSP00000368933.3:p.Val192=
ENST00000466073.5:c.570C>G (TFAP2A) ENSP00000417495.1:p.Val190=
ENST00000473652.1:n.624C>G (TFAP2A)
ENST00000475264.5:c.284C>G (TFAP2A)
ENST00000478375.5:n.570C>G (TFAP2A)
ENST00000482890.5:c.570C>G (TFAP2A) ENSP00000418541.1:p.Val190=
ENST00000488193.5:c.*67C>G (TFAP2A) ENSP00000419823.1:n.*67C>G
ENST00000489805.5:c.*67C>G (TFAP2A) ENSP00000420568.1:n.*67C>G
ENST00000490875.5:n.812C>G (TFAP2A)
ENST00000497266.5:n.541C>G (TFAP2A)
ENST00000498450.1:c.141C>G (TFAP2A) ENSP00000419961.1:p.Val47=
NM_001032280.2:c.552C>G (TFAP2A) NP_001027451.1:p.Val184=
NM_001042425.1:c.558C>G (TFAP2A) NP_001035890.1:p.Val186=
NM_003220.2:c.570C>G (TFAP2A) NP_003211.1:p.Val190=
XM_006715175.2:c.705C>G (TFAP2A) XP_006715238.1:p.Val235=
XM_011514833.1:c.420C>G (TFAP2A) XP_011513135.1:p.Val140=
NR_145448.1:n.201G>C (TFAP2A-AS2)
XM_011514833.2:c.420C>G (TFAP2A) XP_011513135.1:p.Val140=
XM_017011232.1:c.816C>G (TFAP2A) XP_016866721.1:p.Val272=
NM_003220.3:c.570C>G (TFAP2A) NP_003211.1:p.Val190=
NM_001032280.3:c.552C>G (TFAP2A) NP_001027451.1:p.Val184=
NM_001042425.2:c.558C>G (TFAP2A) NP_001035890.1:p.Val186=
NM_001372066.1:c.576C>G (TFAP2A) MANE Select NP_001358995.1:p.Val192=
NM_001042425.3:c.558C>G (TFAP2A) NP_001035890.1:p.Val186=