Canonical Allele Identifier: CA362702730

Gene: TFAP2A TFAP2A-AS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10406829C>T , CM000668.2:g.10406829C>T	GRCh38
NC_000006.11:g.10407062C>T , CM000668.1:g.10407062C>T	GRCh37
NC_000006.10:g.10515048C>T	NCBI36
NG_016151.1:g.17736G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.478G>A (TFAP2A)	ENSP00000368928.3:p.Gly160Ser
ENST00000379613.10:c.502G>A (TFAP2A) MANE Select	ENSP00000368933.5:p.Gly168Ser
ENST00000482890.6:c.502G>A (TFAP2A)	ENSP00000418541.2:p.Gly168Ser
ENST00000488193.7:c.359G>A (TFAP2A)	ENSP00000419823.3:p.Gly120Glu
ENST00000498450.3:c.67G>A (TFAP2A)	ENSP00000419961.3:p.Gly23Ser
ENST00000319516.8:c.484G>A (TFAP2A)	ENSP00000316516.4:p.Gly162Ser
ENST00000379608.7:c.478G>A (TFAP2A)	ENSP00000368928.3:p.Gly160Ser
ENST00000379613.7:c.502G>A (TFAP2A)	ENSP00000368933.3:p.Gly168Ser
ENST00000462727.1:n.534G>A (TFAP2A)
ENST00000466073.5:c.496G>A (TFAP2A)	ENSP00000417495.1:p.Gly166Ser
ENST00000473652.1:n.550G>A (TFAP2A)
ENST00000474952.5:n.928G>A (TFAP2A)
ENST00000475264.5:c.210G>A (TFAP2A)
ENST00000478375.5:n.496G>A (TFAP2A)
ENST00000482890.5:c.496G>A (TFAP2A)	ENSP00000418541.1:p.Gly166Ser
ENST00000488193.5:c.359G>A (TFAP2A)	ENSP00000419823.1:p.Gly120Glu
ENST00000489805.5:c.335G>A (TFAP2A)	ENSP00000420568.1:p.Gly112Glu
ENST00000490875.5:n.738G>A (TFAP2A)
ENST00000497266.5:n.467G>A (TFAP2A)
ENST00000498450.1:c.67G>A (TFAP2A)	ENSP00000419961.1:p.Gly23Ser
NM_001032280.2:c.478G>A (TFAP2A)	NP_001027451.1:p.Gly160Ser
NM_001042425.1:c.484G>A (TFAP2A)	NP_001035890.1:p.Gly162Ser
NM_003220.2:c.496G>A (TFAP2A)	NP_003211.1:p.Gly166Ser
XM_006715175.2:c.631G>A (TFAP2A)	XP_006715238.1:p.Gly211Ser
XM_011514833.1:c.346G>A (TFAP2A)	XP_011513135.1:p.Gly116Ser
NR_145448.1:n.2328C>T (TFAP2A-AS2)
XM_011514833.2:c.346G>A (TFAP2A)	XP_011513135.1:p.Gly116Ser
XM_017011232.1:c.742G>A (TFAP2A)	XP_016866721.1:p.Gly248Ser
NM_003220.3:c.496G>A (TFAP2A)	NP_003211.1:p.Gly166Ser
NM_001032280.3:c.478G>A (TFAP2A)	NP_001027451.1:p.Gly160Ser
NM_001042425.2:c.484G>A (TFAP2A)	NP_001035890.1:p.Gly162Ser
NM_001372066.1:c.502G>A (TFAP2A) MANE Select	NP_001358995.1:p.Gly168Ser
NM_001042425.3:c.484G>A (TFAP2A)	NP_001035890.1:p.Gly162Ser