Canonical Allele Identifier: CA362701707

Gene: TFAP2A TFAP2A-AS2

Linked Data

• MyVariant Identifiers: chr6:g.10404909T>G (hg19) ; chr6:g.10404676T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404676T>G , CM000668.2:g.10404676T>G	GRCh38
NC_000006.11:g.10404909T>G , CM000668.1:g.10404909T>G	GRCh37
NC_000006.10:g.10512895T>G	NCBI36
NG_016151.1:g.19889A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.578A>C (TFAP2A)	ENSP00000368928.3:p.Asn193Thr
ENST00000379613.10:c.602A>C (TFAP2A) MANE Select	ENSP00000368933.5:p.Asn201Thr
ENST00000482890.6:c.602A>C (TFAP2A)	ENSP00000418541.2:p.Asn201Thr
ENST00000488193.7:c.*93A>C (TFAP2A)	ENSP00000419823.3:n.*93A>C
ENST00000498450.3:c.167A>C (TFAP2A)	ENSP00000419961.3:p.Asn56Thr
ENST00000319516.8:c.584A>C (TFAP2A)	ENSP00000316516.4:p.Asn195Thr
ENST00000379608.7:c.578A>C (TFAP2A)	ENSP00000368928.3:p.Asn193Thr
ENST00000379613.7:c.602A>C (TFAP2A)	ENSP00000368933.3:p.Asn201Thr
ENST00000466073.5:c.596A>C (TFAP2A)	ENSP00000417495.1:p.Asn199Thr
ENST00000473652.1:n.650A>C (TFAP2A)
ENST00000475264.5:c.310A>C (TFAP2A)
ENST00000478375.5:n.596A>C (TFAP2A)
ENST00000482890.5:c.596A>C (TFAP2A)	ENSP00000418541.1:p.Asn199Thr
ENST00000488193.5:c.*93A>C (TFAP2A)	ENSP00000419823.1:n.*93A>C
ENST00000489805.5:c.*93A>C (TFAP2A)	ENSP00000420568.1:n.*93A>C
ENST00000490875.5:n.838A>C (TFAP2A)
ENST00000497266.5:n.567A>C (TFAP2A)
ENST00000498450.1:c.167A>C (TFAP2A)	ENSP00000419961.1:p.Asn56Thr
NM_001032280.2:c.578A>C (TFAP2A)	NP_001027451.1:p.Asn193Thr
NM_001042425.1:c.584A>C (TFAP2A)	NP_001035890.1:p.Asn195Thr
NM_003220.2:c.596A>C (TFAP2A)	NP_003211.1:p.Asn199Thr
XM_006715175.2:c.731A>C (TFAP2A)	XP_006715238.1:p.Asn244Thr
XM_011514833.1:c.446A>C (TFAP2A)	XP_011513135.1:p.Asn149Thr
NR_145448.1:n.175T>G (TFAP2A-AS2)
XM_011514833.2:c.446A>C (TFAP2A)	XP_011513135.1:p.Asn149Thr
XM_017011232.1:c.842A>C (TFAP2A)	XP_016866721.1:p.Asn281Thr
NM_003220.3:c.596A>C (TFAP2A)	NP_003211.1:p.Asn199Thr
NM_001032280.3:c.578A>C (TFAP2A)	NP_001027451.1:p.Asn193Thr
NM_001042425.2:c.584A>C (TFAP2A)	NP_001035890.1:p.Asn195Thr
NM_001372066.1:c.602A>C (TFAP2A) MANE Select	NP_001358995.1:p.Asn201Thr
NM_001042425.3:c.584A>C (TFAP2A)	NP_001035890.1:p.Asn195Thr