Canonical Allele Identifier: CA448717652
Gene: TFAP2A HGNC NCBI
TFAP2A-AS2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.10404842G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10404609G>T , CM000668.2:g.10404609G>T GRCh38
NC_000006.11:g.10404842G>T , CM000668.1:g.10404842G>T GRCh37
NC_000006.10:g.10512828G>T NCBI36
NG_016151.1:g.19956C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000379608.9:c.645C>A (TFAP2A) ENSP00000368928.3:p.Leu215=
ENST00000379613.10:c.669C>A (TFAP2A) MANE Select ENSP00000368933.5:p.Leu223=
ENST00000482890.6:c.669C>A (TFAP2A) ENSP00000418541.2:p.Leu223=
ENST00000488193.7:c.*160C>A (TFAP2A) ENSP00000419823.3:n.*160C>A
ENST00000498450.3:c.234C>A (TFAP2A) ENSP00000419961.3:p.Leu78=
ENST00000319516.8:c.651C>A (TFAP2A) ENSP00000316516.4:p.Leu217=
ENST00000379608.7:c.645C>A (TFAP2A) ENSP00000368928.3:p.Leu215=
ENST00000379613.7:c.669C>A (TFAP2A) ENSP00000368933.3:p.Leu223=
ENST00000466073.5:c.663C>A (TFAP2A) ENSP00000417495.1:p.Leu221=
ENST00000475264.5:c.377C>A (TFAP2A)
ENST00000478375.5:n.663C>A (TFAP2A)
ENST00000482890.5:c.663C>A (TFAP2A) ENSP00000418541.1:p.Leu221=
ENST00000488193.5:c.*160C>A (TFAP2A) ENSP00000419823.1:n.*160C>A
ENST00000489805.5:c.*160C>A (TFAP2A) ENSP00000420568.1:n.*160C>A
ENST00000497266.5:n.634C>A (TFAP2A)
ENST00000498450.1:c.234C>A (TFAP2A) ENSP00000419961.1:p.Leu78=
NM_001032280.2:c.645C>A (TFAP2A) NP_001027451.1:p.Leu215=
NM_001042425.1:c.651C>A (TFAP2A) NP_001035890.1:p.Leu217=
NM_003220.2:c.663C>A (TFAP2A) NP_003211.1:p.Leu221=
XM_006715175.2:c.798C>A (TFAP2A) XP_006715238.1:p.Leu266=
XM_011514833.1:c.513C>A (TFAP2A) XP_011513135.1:p.Leu171=
NR_145448.1:n.108G>T (TFAP2A-AS2)
XM_011514833.2:c.513C>A (TFAP2A) XP_011513135.1:p.Leu171=
XM_017011232.1:c.909C>A (TFAP2A) XP_016866721.1:p.Leu303=
NM_003220.3:c.663C>A (TFAP2A) NP_003211.1:p.Leu221=
NM_001032280.3:c.645C>A (TFAP2A) NP_001027451.1:p.Leu215=
NM_001042425.2:c.651C>A (TFAP2A) NP_001035890.1:p.Leu217=
NM_001372066.1:c.669C>A (TFAP2A) MANE Select NP_001358995.1:p.Leu223=
NM_001042425.3:c.651C>A (TFAP2A) NP_001035890.1:p.Leu217=