Canonical Allele Identifier: CA362701781

Gene: TFAP2A TFAP2A-AS2

Linked Data

• MyVariant Identifiers: chr6:g.10404924G>T (hg19) ; chr6:g.10404691G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404691G>T , CM000668.2:g.10404691G>T	GRCh38
NC_000006.11:g.10404924G>T , CM000668.1:g.10404924G>T	GRCh37
NC_000006.10:g.10512910G>T	NCBI36
NG_016151.1:g.19874C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.563C>A (TFAP2A)	ENSP00000368928.3:p.Pro188His
ENST00000379613.10:c.587C>A (TFAP2A) MANE Select	ENSP00000368933.5:p.Pro196His
ENST00000482890.6:c.587C>A (TFAP2A)	ENSP00000418541.2:p.Pro196His
ENST00000488193.7:c.*78C>A (TFAP2A)	ENSP00000419823.3:n.*78C>A
ENST00000498450.3:c.152C>A (TFAP2A)	ENSP00000419961.3:p.Pro51His
ENST00000319516.8:c.569C>A (TFAP2A)	ENSP00000316516.4:p.Pro190His
ENST00000379608.7:c.563C>A (TFAP2A)	ENSP00000368928.3:p.Pro188His
ENST00000379613.7:c.587C>A (TFAP2A)	ENSP00000368933.3:p.Pro196His
ENST00000466073.5:c.581C>A (TFAP2A)	ENSP00000417495.1:p.Pro194His
ENST00000473652.1:n.635C>A (TFAP2A)
ENST00000475264.5:c.295C>A (TFAP2A)
ENST00000478375.5:n.581C>A (TFAP2A)
ENST00000482890.5:c.581C>A (TFAP2A)	ENSP00000418541.1:p.Pro194His
ENST00000488193.5:c.*78C>A (TFAP2A)	ENSP00000419823.1:n.*78C>A
ENST00000489805.5:c.*78C>A (TFAP2A)	ENSP00000420568.1:n.*78C>A
ENST00000490875.5:n.823C>A (TFAP2A)
ENST00000497266.5:n.552C>A (TFAP2A)
ENST00000498450.1:c.152C>A (TFAP2A)	ENSP00000419961.1:p.Pro51His
NM_001032280.2:c.563C>A (TFAP2A)	NP_001027451.1:p.Pro188His
NM_001042425.1:c.569C>A (TFAP2A)	NP_001035890.1:p.Pro190His
NM_003220.2:c.581C>A (TFAP2A)	NP_003211.1:p.Pro194His
XM_006715175.2:c.716C>A (TFAP2A)	XP_006715238.1:p.Pro239His
XM_011514833.1:c.431C>A (TFAP2A)	XP_011513135.1:p.Pro144His
NR_145448.1:n.190G>T (TFAP2A-AS2)
XM_011514833.2:c.431C>A (TFAP2A)	XP_011513135.1:p.Pro144His
XM_017011232.1:c.827C>A (TFAP2A)	XP_016866721.1:p.Pro276His
NM_003220.3:c.581C>A (TFAP2A)	NP_003211.1:p.Pro194His
NM_001032280.3:c.563C>A (TFAP2A)	NP_001027451.1:p.Pro188His
NM_001042425.2:c.569C>A (TFAP2A)	NP_001035890.1:p.Pro190His
NM_001372066.1:c.587C>A (TFAP2A) MANE Select	NP_001358995.1:p.Pro196His
NM_001042425.3:c.569C>A (TFAP2A)	NP_001035890.1:p.Pro190His