Canonical Allele Identifier: CA448717471

Gene: TFAP2A TFAP2A-AS2

Linked Data

• dbSNP Id: rs1221567277
• gnomAD v2: 6-10404767-C-T
• gnomAD v4: 6-10404534-C-T
• MyVariant Identifiers: chr6:g.10404767C>T (hg19) ; chr6:g.10404534C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404534C>T , CM000668.2:g.10404534C>T	GRCh38
NC_000006.11:g.10404767C>T , CM000668.1:g.10404767C>T	GRCh37
NC_000006.10:g.10512753C>T	NCBI36
NG_016151.1:g.20031G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.720G>A (TFAP2A)	ENSP00000368928.3:p.Ala240=
ENST00000379613.10:c.744G>A (TFAP2A) MANE Select	ENSP00000368933.5:p.Ala248=
ENST00000482890.6:c.744G>A (TFAP2A)	ENSP00000418541.2:p.Ala248=
ENST00000488193.7:c.*235G>A (TFAP2A)	ENSP00000419823.3:n.*235G>A
ENST00000498450.3:c.309G>A (TFAP2A)	ENSP00000419961.3:p.Ala103=
ENST00000319516.8:c.726G>A (TFAP2A)	ENSP00000316516.4:p.Ala242=
ENST00000379608.7:c.720G>A (TFAP2A)	ENSP00000368928.3:p.Ala240=
ENST00000379613.7:c.744G>A (TFAP2A)	ENSP00000368933.3:p.Ala248=
ENST00000461628.5:c.61G>A (TFAP2A)
ENST00000466073.5:c.738G>A (TFAP2A)	ENSP00000417495.1:p.Ala246=
ENST00000475264.5:c.452G>A (TFAP2A)
ENST00000478375.5:n.738G>A (TFAP2A)
ENST00000482890.5:c.738G>A (TFAP2A)	ENSP00000418541.1:p.Ala246=
ENST00000488193.5:c.*235G>A (TFAP2A)	ENSP00000419823.1:n.*235G>A
ENST00000489805.5:c.*235G>A (TFAP2A)	ENSP00000420568.1:n.*235G>A
ENST00000497266.5:n.709G>A (TFAP2A)
ENST00000498450.1:c.309G>A (TFAP2A)	ENSP00000419961.1:p.Ala103=
NM_001032280.2:c.720G>A (TFAP2A)	NP_001027451.1:p.Ala240=
NM_001042425.1:c.726G>A (TFAP2A)	NP_001035890.1:p.Ala242=
NM_003220.2:c.738G>A (TFAP2A)	NP_003211.1:p.Ala246=
XM_006715175.2:c.873G>A (TFAP2A)	XP_006715238.1:p.Ala291=
XM_011514833.1:c.588G>A (TFAP2A)	XP_011513135.1:p.Ala196=
NR_145448.1:n.33C>T (TFAP2A-AS2)
XM_011514833.2:c.588G>A (TFAP2A)	XP_011513135.1:p.Ala196=
XM_017011232.1:c.984G>A (TFAP2A)	XP_016866721.1:p.Ala328=
NM_003220.3:c.738G>A (TFAP2A)	NP_003211.1:p.Ala246=
NM_001032280.3:c.720G>A (TFAP2A)	NP_001027451.1:p.Ala240=
NM_001042425.2:c.726G>A (TFAP2A)	NP_001035890.1:p.Ala242=
NM_001372066.1:c.744G>A (TFAP2A) MANE Select	NP_001358995.1:p.Ala248=
NM_001042425.3:c.726G>A (TFAP2A)	NP_001035890.1:p.Ala242=