Canonical Allele Identifier: CA1609976751

Gene: TFAP2A TFAP2A-AS2

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404568T= , CM000668.2:g.10404568T=	GRCh38
NC_000006.11:g.10404801T= , CM000668.1:g.10404801T=	GRCh37
NC_000006.10:g.10512787T=	NCBI36
NG_016151.1:g.19997A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.686A= (TFAP2A)	ENSP00000368928.3:p.Gln229=
ENST00000379613.10:c.710A= (TFAP2A) MANE Select	ENSP00000368933.5:p.Gln237=
ENST00000482890.6:c.710A= (TFAP2A)	ENSP00000418541.2:p.Gln237=
ENST00000488193.7:c.*201A= (TFAP2A)	ENSP00000419823.3:n.*201A=
ENST00000498450.3:c.275A= (TFAP2A)	ENSP00000419961.3:p.Gln92=
ENST00000319516.8:c.692A= (TFAP2A)	ENSP00000316516.4:p.Gln231=
ENST00000379608.7:c.686A= (TFAP2A)	ENSP00000368928.3:p.Gln229=
ENST00000379613.7:c.710A= (TFAP2A)	ENSP00000368933.3:p.Gln237=
ENST00000461628.5:c.27A= (TFAP2A)
ENST00000466073.5:c.704A= (TFAP2A)	ENSP00000417495.1:p.Gln235=
ENST00000475264.5:c.418A= (TFAP2A)
ENST00000478375.5:n.704A= (TFAP2A)
ENST00000482890.5:c.704A= (TFAP2A)	ENSP00000418541.1:p.Gln235=
ENST00000488193.5:c.*201A= (TFAP2A)	ENSP00000419823.1:n.*201A=
ENST00000489805.5:c.*201A= (TFAP2A)	ENSP00000420568.1:n.*201A=
ENST00000497266.5:n.675A= (TFAP2A)
ENST00000498450.1:c.275A= (TFAP2A)	ENSP00000419961.1:p.Gln92=
NM_001032280.2:c.686A= (TFAP2A)	NP_001027451.1:p.Gln229=
NM_001042425.1:c.692A= (TFAP2A)	NP_001035890.1:p.Gln231=
NM_003220.2:c.704A= (TFAP2A)	NP_003211.1:p.Gln235=
XM_006715175.2:c.839A= (TFAP2A)	XP_006715238.1:p.Gln280=
XM_011514833.1:c.554A= (TFAP2A)	XP_011513135.1:p.Gln185=
NR_145448.1:n.67T= (TFAP2A-AS2)
XM_011514833.2:c.554A= (TFAP2A)	XP_011513135.1:p.Gln185=
XM_017011232.1:c.950A= (TFAP2A)	XP_016866721.1:p.Gln317=
NM_003220.3:c.704A= (TFAP2A)	NP_003211.1:p.Gln235=
NM_001032280.3:c.686A= (TFAP2A)	NP_001027451.1:p.Gln229=
NM_001042425.2:c.692A= (TFAP2A)	NP_001035890.1:p.Gln231=
NM_001372066.1:c.710A= (TFAP2A) MANE Select	NP_001358995.1:p.Gln237=
NM_001042425.3:c.692A= (TFAP2A)	NP_001035890.1:p.Gln231=