Canonical Allele Identifier: CA3631260

Gene: TFAP2A TFAP2A-AS2

Linked Data

• dbSNP Id: rs121909574
• ExAC: 6:10404742 T / G
• gnomAD v2: 6-10404742-T-G
• gnomAD v3: 6-10404509-T-G
• gnomAD v4: 6-10404509-T-G
• MyVariant Identifiers: chr6:g.10404742T>G (hg19) ; chr6:g.10404509T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404509T>G , CM000668.2:g.10404509T>G	GRCh38
NC_000006.11:g.10404742T>G , CM000668.1:g.10404742T>G	GRCh37
NC_000006.10:g.10512728T>G	NCBI36
NG_016151.1:g.20056A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.745A>C (TFAP2A)	ENSP00000368928.3:p.Arg249=
ENST00000379613.10:c.769A>C (TFAP2A) MANE Select	ENSP00000368933.5:p.Arg257=
ENST00000482890.6:c.769A>C (TFAP2A)	ENSP00000418541.2:p.Arg257=
ENST00000488193.7:c.*260A>C (TFAP2A)	ENSP00000419823.3:n.*260A>C
ENST00000498450.3:c.334A>C (TFAP2A)	ENSP00000419961.3:p.Arg112=
ENST00000319516.8:c.751A>C (TFAP2A)	ENSP00000316516.4:p.Arg251=
ENST00000379608.7:c.745A>C (TFAP2A)	ENSP00000368928.3:p.Arg249=
ENST00000379613.7:c.769A>C (TFAP2A)	ENSP00000368933.3:p.Arg257=
ENST00000461628.5:c.86A>C (TFAP2A)
ENST00000466073.5:c.763A>C (TFAP2A)	ENSP00000417495.1:p.Arg255=
ENST00000475264.5:c.477A>C (TFAP2A)
ENST00000478375.5:n.763A>C (TFAP2A)
ENST00000482890.5:c.763A>C (TFAP2A)	ENSP00000418541.1:p.Arg255=
ENST00000488193.5:c.*260A>C (TFAP2A)	ENSP00000419823.1:n.*260A>C
ENST00000489805.5:c.*260A>C (TFAP2A)	ENSP00000420568.1:n.*260A>C
ENST00000497266.5:n.734A>C (TFAP2A)
ENST00000498450.1:c.334A>C (TFAP2A)	ENSP00000419961.1:p.Arg112=
NM_001032280.2:c.745A>C (TFAP2A)	NP_001027451.1:p.Arg249=
NM_001042425.1:c.751A>C (TFAP2A)	NP_001035890.1:p.Arg251=
NM_003220.2:c.763A>C (TFAP2A)	NP_003211.1:p.Arg255=
XM_006715175.2:c.898A>C (TFAP2A)	XP_006715238.1:p.Arg300=
XM_011514833.1:c.613A>C (TFAP2A)	XP_011513135.1:p.Arg205=
NR_145448.1:n.8T>G (TFAP2A-AS2)
XM_011514833.2:c.613A>C (TFAP2A)	XP_011513135.1:p.Arg205=
XM_017011232.1:c.1009A>C (TFAP2A)	XP_016866721.1:p.Arg337=
NM_003220.3:c.763A>C (TFAP2A)	NP_003211.1:p.Arg255=
NM_001032280.3:c.745A>C (TFAP2A)	NP_001027451.1:p.Arg249=
NM_001042425.2:c.751A>C (TFAP2A)	NP_001035890.1:p.Arg251=
NM_001372066.1:c.769A>C (TFAP2A) MANE Select	NP_001358995.1:p.Arg257=
NM_001042425.3:c.751A>C (TFAP2A)	NP_001035890.1:p.Arg251=