Canonical Allele Identifier: CA362701181

Gene: TFAP2A TFAP2A-AS2

Linked Data

• MyVariant Identifiers: chr6:g.10404766A>T (hg19) ; chr6:g.10404533A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404533A>T , CM000668.2:g.10404533A>T	GRCh38
NC_000006.11:g.10404766A>T , CM000668.1:g.10404766A>T	GRCh37
NC_000006.10:g.10512752A>T	NCBI36
NG_016151.1:g.20032T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.721T>A (TFAP2A)	ENSP00000368928.3:p.Ser241Thr
ENST00000379613.10:c.745T>A (TFAP2A) MANE Select	ENSP00000368933.5:p.Ser249Thr
ENST00000482890.6:c.745T>A (TFAP2A)	ENSP00000418541.2:p.Ser249Thr
ENST00000488193.7:c.*236T>A (TFAP2A)	ENSP00000419823.3:n.*236T>A
ENST00000498450.3:c.310T>A (TFAP2A)	ENSP00000419961.3:p.Ser104Thr
ENST00000319516.8:c.727T>A (TFAP2A)	ENSP00000316516.4:p.Ser243Thr
ENST00000379608.7:c.721T>A (TFAP2A)	ENSP00000368928.3:p.Ser241Thr
ENST00000379613.7:c.745T>A (TFAP2A)	ENSP00000368933.3:p.Ser249Thr
ENST00000461628.5:c.62T>A (TFAP2A)
ENST00000466073.5:c.739T>A (TFAP2A)	ENSP00000417495.1:p.Ser247Thr
ENST00000475264.5:c.453T>A (TFAP2A)
ENST00000478375.5:n.739T>A (TFAP2A)
ENST00000482890.5:c.739T>A (TFAP2A)	ENSP00000418541.1:p.Ser247Thr
ENST00000488193.5:c.*236T>A (TFAP2A)	ENSP00000419823.1:n.*236T>A
ENST00000489805.5:c.*236T>A (TFAP2A)	ENSP00000420568.1:n.*236T>A
ENST00000497266.5:n.710T>A (TFAP2A)
ENST00000498450.1:c.310T>A (TFAP2A)	ENSP00000419961.1:p.Ser104Thr
NM_001032280.2:c.721T>A (TFAP2A)	NP_001027451.1:p.Ser241Thr
NM_001042425.1:c.727T>A (TFAP2A)	NP_001035890.1:p.Ser243Thr
NM_003220.2:c.739T>A (TFAP2A)	NP_003211.1:p.Ser247Thr
XM_006715175.2:c.874T>A (TFAP2A)	XP_006715238.1:p.Ser292Thr
XM_011514833.1:c.589T>A (TFAP2A)	XP_011513135.1:p.Ser197Thr
NR_145448.1:n.32A>T (TFAP2A-AS2)
XM_011514833.2:c.589T>A (TFAP2A)	XP_011513135.1:p.Ser197Thr
XM_017011232.1:c.985T>A (TFAP2A)	XP_016866721.1:p.Ser329Thr
NM_003220.3:c.739T>A (TFAP2A)	NP_003211.1:p.Ser247Thr
NM_001032280.3:c.721T>A (TFAP2A)	NP_001027451.1:p.Ser241Thr
NM_001042425.2:c.727T>A (TFAP2A)	NP_001035890.1:p.Ser243Thr
NM_001372066.1:c.745T>A (TFAP2A) MANE Select	NP_001358995.1:p.Ser249Thr
NM_001042425.3:c.727T>A (TFAP2A)	NP_001035890.1:p.Ser243Thr