Canonical Allele Identifier: CA362701433

Gene: TFAP2A TFAP2A-AS2

Linked Data

• MyVariant Identifiers: chr6:g.10404839G>C (hg19) ; chr6:g.10404606G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404606G>C , CM000668.2:g.10404606G>C	GRCh38
NC_000006.11:g.10404839G>C , CM000668.1:g.10404839G>C	GRCh37
NC_000006.10:g.10512825G>C	NCBI36
NG_016151.1:g.19959C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.648C>G (TFAP2A)	ENSP00000368928.3:p.Ser216Arg
ENST00000379613.10:c.672C>G (TFAP2A) MANE Select	ENSP00000368933.5:p.Ser224Arg
ENST00000482890.6:c.672C>G (TFAP2A)	ENSP00000418541.2:p.Ser224Arg
ENST00000488193.7:c.*163C>G (TFAP2A)	ENSP00000419823.3:n.*163C>G
ENST00000498450.3:c.237C>G (TFAP2A)	ENSP00000419961.3:p.Ser79Arg
ENST00000319516.8:c.654C>G (TFAP2A)	ENSP00000316516.4:p.Ser218Arg
ENST00000379608.7:c.648C>G (TFAP2A)	ENSP00000368928.3:p.Ser216Arg
ENST00000379613.7:c.672C>G (TFAP2A)	ENSP00000368933.3:p.Ser224Arg
ENST00000466073.5:c.666C>G (TFAP2A)	ENSP00000417495.1:p.Ser222Arg
ENST00000475264.5:c.380C>G (TFAP2A)
ENST00000478375.5:n.666C>G (TFAP2A)
ENST00000482890.5:c.666C>G (TFAP2A)	ENSP00000418541.1:p.Ser222Arg
ENST00000488193.5:c.*163C>G (TFAP2A)	ENSP00000419823.1:n.*163C>G
ENST00000489805.5:c.*163C>G (TFAP2A)	ENSP00000420568.1:n.*163C>G
ENST00000497266.5:n.637C>G (TFAP2A)
ENST00000498450.1:c.237C>G (TFAP2A)	ENSP00000419961.1:p.Ser79Arg
NM_001032280.2:c.648C>G (TFAP2A)	NP_001027451.1:p.Ser216Arg
NM_001042425.1:c.654C>G (TFAP2A)	NP_001035890.1:p.Ser218Arg
NM_003220.2:c.666C>G (TFAP2A)	NP_003211.1:p.Ser222Arg
XM_006715175.2:c.801C>G (TFAP2A)	XP_006715238.1:p.Ser267Arg
XM_011514833.1:c.516C>G (TFAP2A)	XP_011513135.1:p.Ser172Arg
NR_145448.1:n.105G>C (TFAP2A-AS2)
XM_011514833.2:c.516C>G (TFAP2A)	XP_011513135.1:p.Ser172Arg
XM_017011232.1:c.912C>G (TFAP2A)	XP_016866721.1:p.Ser304Arg
NM_003220.3:c.666C>G (TFAP2A)	NP_003211.1:p.Ser222Arg
NM_001032280.3:c.648C>G (TFAP2A)	NP_001027451.1:p.Ser216Arg
NM_001042425.2:c.654C>G (TFAP2A)	NP_001035890.1:p.Ser218Arg
NM_001372066.1:c.672C>G (TFAP2A) MANE Select	NP_001358995.1:p.Ser224Arg
NM_001042425.3:c.654C>G (TFAP2A)	NP_001035890.1:p.Ser218Arg