Canonical Allele Identifier: CA448717500

Gene: TFAP2A TFAP2A-AS2

Linked Data

• MyVariant Identifiers: chr6:g.10404785T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404552T>G , CM000668.2:g.10404552T>G	GRCh38
NC_000006.11:g.10404785T>G , CM000668.1:g.10404785T>G	GRCh37
NC_000006.10:g.10512771T>G	NCBI36
NG_016151.1:g.20013A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.702A>C (TFAP2A)	ENSP00000368928.3:p.Pro234=
ENST00000379613.10:c.726A>C (TFAP2A) MANE Select	ENSP00000368933.5:p.Pro242=
ENST00000482890.6:c.726A>C (TFAP2A)	ENSP00000418541.2:p.Pro242=
ENST00000488193.7:c.*217A>C (TFAP2A)	ENSP00000419823.3:n.*217A>C
ENST00000498450.3:c.291A>C (TFAP2A)	ENSP00000419961.3:p.Pro97=
ENST00000319516.8:c.708A>C (TFAP2A)	ENSP00000316516.4:p.Pro236=
ENST00000379608.7:c.702A>C (TFAP2A)	ENSP00000368928.3:p.Pro234=
ENST00000379613.7:c.726A>C (TFAP2A)	ENSP00000368933.3:p.Pro242=
ENST00000461628.5:c.43A>C (TFAP2A)
ENST00000466073.5:c.720A>C (TFAP2A)	ENSP00000417495.1:p.Pro240=
ENST00000475264.5:c.434A>C (TFAP2A)
ENST00000478375.5:n.720A>C (TFAP2A)
ENST00000482890.5:c.720A>C (TFAP2A)	ENSP00000418541.1:p.Pro240=
ENST00000488193.5:c.*217A>C (TFAP2A)	ENSP00000419823.1:n.*217A>C
ENST00000489805.5:c.*217A>C (TFAP2A)	ENSP00000420568.1:n.*217A>C
ENST00000497266.5:n.691A>C (TFAP2A)
ENST00000498450.1:c.291A>C (TFAP2A)	ENSP00000419961.1:p.Pro97=
NM_001032280.2:c.702A>C (TFAP2A)	NP_001027451.1:p.Pro234=
NM_001042425.1:c.708A>C (TFAP2A)	NP_001035890.1:p.Pro236=
NM_003220.2:c.720A>C (TFAP2A)	NP_003211.1:p.Pro240=
XM_006715175.2:c.855A>C (TFAP2A)	XP_006715238.1:p.Pro285=
XM_011514833.1:c.570A>C (TFAP2A)	XP_011513135.1:p.Pro190=
NR_145448.1:n.51T>G (TFAP2A-AS2)
XM_011514833.2:c.570A>C (TFAP2A)	XP_011513135.1:p.Pro190=
XM_017011232.1:c.966A>C (TFAP2A)	XP_016866721.1:p.Pro322=
NM_003220.3:c.720A>C (TFAP2A)	NP_003211.1:p.Pro240=
NM_001032280.3:c.702A>C (TFAP2A)	NP_001027451.1:p.Pro234=
NM_001042425.2:c.708A>C (TFAP2A)	NP_001035890.1:p.Pro236=
NM_001372066.1:c.726A>C (TFAP2A) MANE Select	NP_001358995.1:p.Pro242=
NM_001042425.3:c.708A>C (TFAP2A)	NP_001035890.1:p.Pro236=