Canonical Allele Identifier: CA134041999

Gene: TFAP2A

Linked Data

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10397883T>G , CM000668.2:g.10397883T>G	GRCh38
NC_000006.11:g.10398116T>G , CM000668.1:g.10398116T>G	GRCh37
NC_000006.10:g.10506102T>G	NCBI36
NG_016151.1:g.26682A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.*534A>C	ENSP00000368928.3:n.*534A>C
ENST00000379613.10:c.*534A>C MANE Select	ENSP00000368933.5:n.*534A>C
ENST00000319516.8:c.*534A>C	ENSP00000316516.4:n.*534A>C
ENST00000379613.7:c.*534A>C	ENSP00000368933.3:n.*534A>C
ENST00000461628.5:c.207-4322A>C
ENST00000489805.5:c.*1345A>C	ENSP00000420568.1:n.*1345A>C
NM_001032280.2:c.*534A>C	NP_001027451.1:n.*534A>C
NM_001042425.1:c.*534A>C	NP_001035890.1:n.*534A>C
NM_003220.2:c.*534A>C	NP_003211.1:n.*534A>C
XM_006715175.2:c.*534A>C	XP_006715238.1:n.*534A>C
XM_011514833.1:c.*534A>C	XP_011513135.1:n.*534A>C
XM_011514833.2:c.*534A>C	XP_011513135.1:n.*534A>C
XM_017011232.1:c.*534A>C	XP_016866721.1:n.*534A>C
NM_003220.3:c.*534A>C	NP_003211.1:n.*534A>C
NM_001032280.3:c.*534A>C	NP_001027451.1:n.*534A>C
NM_001042425.2:c.*534A>C	NP_001035890.1:n.*534A>C
NM_001372066.1:c.*534A>C MANE Select	NP_001358995.1:n.*534A>C
NM_001042425.3:c.*534A>C	NP_001035890.1:n.*534A>C