Canonical Allele Identifier: CA362701964

Gene: TFAP2A TFAP2A-AS2

Linked Data

• MyVariant Identifiers: chr6:g.10404969G>C (hg19) ; chr6:g.10404736G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404736G>C , CM000668.2:g.10404736G>C	GRCh38
NC_000006.11:g.10404969G>C , CM000668.1:g.10404969G>C	GRCh37
NC_000006.10:g.10512955G>C	NCBI36
NG_016151.1:g.19829C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.518C>G (TFAP2A)	ENSP00000368928.3:p.Pro173Arg
ENST00000379613.10:c.542C>G (TFAP2A) MANE Select	ENSP00000368933.5:p.Pro181Arg
ENST00000482890.6:c.542C>G (TFAP2A)	ENSP00000418541.2:p.Pro181Arg
ENST00000488193.7:c.*33C>G (TFAP2A)	ENSP00000419823.3:n.*33C>G
ENST00000498450.3:c.107C>G (TFAP2A)	ENSP00000419961.3:p.Pro36Arg
ENST00000319516.8:c.524C>G (TFAP2A)	ENSP00000316516.4:p.Pro175Arg
ENST00000379608.7:c.518C>G (TFAP2A)	ENSP00000368928.3:p.Pro173Arg
ENST00000379613.7:c.542C>G (TFAP2A)	ENSP00000368933.3:p.Pro181Arg
ENST00000466073.5:c.536C>G (TFAP2A)	ENSP00000417495.1:p.Pro179Arg
ENST00000473652.1:n.590C>G (TFAP2A)
ENST00000475264.5:c.250C>G (TFAP2A)
ENST00000478375.5:n.536C>G (TFAP2A)
ENST00000482890.5:c.536C>G (TFAP2A)	ENSP00000418541.1:p.Pro179Arg
ENST00000488193.5:c.*33C>G (TFAP2A)	ENSP00000419823.1:n.*33C>G
ENST00000489805.5:c.*33C>G (TFAP2A)	ENSP00000420568.1:n.*33C>G
ENST00000490875.5:n.778C>G (TFAP2A)
ENST00000497266.5:n.507C>G (TFAP2A)
ENST00000498450.1:c.107C>G (TFAP2A)	ENSP00000419961.1:p.Pro36Arg
NM_001032280.2:c.518C>G (TFAP2A)	NP_001027451.1:p.Pro173Arg
NM_001042425.1:c.524C>G (TFAP2A)	NP_001035890.1:p.Pro175Arg
NM_003220.2:c.536C>G (TFAP2A)	NP_003211.1:p.Pro179Arg
XM_006715175.2:c.671C>G (TFAP2A)	XP_006715238.1:p.Pro224Arg
XM_011514833.1:c.386C>G (TFAP2A)	XP_011513135.1:p.Pro129Arg
NR_145448.1:n.235G>C (TFAP2A-AS2)
XM_011514833.2:c.386C>G (TFAP2A)	XP_011513135.1:p.Pro129Arg
XM_017011232.1:c.782C>G (TFAP2A)	XP_016866721.1:p.Pro261Arg
NM_003220.3:c.536C>G (TFAP2A)	NP_003211.1:p.Pro179Arg
NM_001032280.3:c.518C>G (TFAP2A)	NP_001027451.1:p.Pro173Arg
NM_001042425.2:c.524C>G (TFAP2A)	NP_001035890.1:p.Pro175Arg
NM_001372066.1:c.542C>G (TFAP2A) MANE Select	NP_001358995.1:p.Pro181Arg
NM_001042425.3:c.524C>G (TFAP2A)	NP_001035890.1:p.Pro175Arg