Canonical Allele Identifier: CA362701968

Gene: TFAP2A TFAP2A-AS2

Linked Data

• MyVariant Identifiers: chr6:g.10404970G>C (hg19) ; chr6:g.10404737G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404737G>C , CM000668.2:g.10404737G>C	GRCh38
NC_000006.11:g.10404970G>C , CM000668.1:g.10404970G>C	GRCh37
NC_000006.10:g.10512956G>C	NCBI36
NG_016151.1:g.19828C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.517C>G (TFAP2A)	ENSP00000368928.3:p.Pro173Ala
ENST00000379613.10:c.541C>G (TFAP2A) MANE Select	ENSP00000368933.5:p.Pro181Ala
ENST00000482890.6:c.541C>G (TFAP2A)	ENSP00000418541.2:p.Pro181Ala
ENST00000488193.7:c.*32C>G (TFAP2A)	ENSP00000419823.3:n.*32C>G
ENST00000498450.3:c.106C>G (TFAP2A)	ENSP00000419961.3:p.Pro36Ala
ENST00000319516.8:c.523C>G (TFAP2A)	ENSP00000316516.4:p.Pro175Ala
ENST00000379608.7:c.517C>G (TFAP2A)	ENSP00000368928.3:p.Pro173Ala
ENST00000379613.7:c.541C>G (TFAP2A)	ENSP00000368933.3:p.Pro181Ala
ENST00000466073.5:c.535C>G (TFAP2A)	ENSP00000417495.1:p.Pro179Ala
ENST00000473652.1:n.589C>G (TFAP2A)
ENST00000475264.5:c.249C>G (TFAP2A)
ENST00000478375.5:n.535C>G (TFAP2A)
ENST00000482890.5:c.535C>G (TFAP2A)	ENSP00000418541.1:p.Pro179Ala
ENST00000488193.5:c.*32C>G (TFAP2A)	ENSP00000419823.1:n.*32C>G
ENST00000489805.5:c.*32C>G (TFAP2A)	ENSP00000420568.1:n.*32C>G
ENST00000490875.5:n.777C>G (TFAP2A)
ENST00000497266.5:n.506C>G (TFAP2A)
ENST00000498450.1:c.106C>G (TFAP2A)	ENSP00000419961.1:p.Pro36Ala
NM_001032280.2:c.517C>G (TFAP2A)	NP_001027451.1:p.Pro173Ala
NM_001042425.1:c.523C>G (TFAP2A)	NP_001035890.1:p.Pro175Ala
NM_003220.2:c.535C>G (TFAP2A)	NP_003211.1:p.Pro179Ala
XM_006715175.2:c.670C>G (TFAP2A)	XP_006715238.1:p.Pro224Ala
XM_011514833.1:c.385C>G (TFAP2A)	XP_011513135.1:p.Pro129Ala
NR_145448.1:n.236G>C (TFAP2A-AS2)
XM_011514833.2:c.385C>G (TFAP2A)	XP_011513135.1:p.Pro129Ala
XM_017011232.1:c.781C>G (TFAP2A)	XP_016866721.1:p.Pro261Ala
NM_003220.3:c.535C>G (TFAP2A)	NP_003211.1:p.Pro179Ala
NM_001032280.3:c.517C>G (TFAP2A)	NP_001027451.1:p.Pro173Ala
NM_001042425.2:c.523C>G (TFAP2A)	NP_001035890.1:p.Pro175Ala
NM_001372066.1:c.541C>G (TFAP2A) MANE Select	NP_001358995.1:p.Pro181Ala
NM_001042425.3:c.523C>G (TFAP2A)	NP_001035890.1:p.Pro175Ala