Canonical Allele Identifier: CA2677252902

Gene: TFAP2A

Linked Data

• gnomAD v4: 6-10404488-G-GGGGCC

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404490_10404494dup , CM000668.2:g.10404490_10404494dup	GRCh38
NC_000006.11:g.10404723_10404727dup , CM000668.1:g.10404723_10404727dup	GRCh37
NC_000006.10:g.10512709_10512713dup	NCBI36
NG_016151.1:g.20072_20076dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.746+15_746+19dup	ENSP00000368928.3:n.746+15_746+19dup
ENST00000379613.10:c.770+15_770+19dup MANE Select	ENSP00000368933.5:n.770+15_770+19dup
ENST00000482890.6:c.770+15_770+19dup	ENSP00000418541.2:n.770+15_770+19dup
ENST00000488193.7:c.*261+15_*261+19dup	ENSP00000419823.3:n.*261+15_*261+19dup
ENST00000498450.3:c.335+15_335+19dup	ENSP00000419961.3:n.335+15_335+19dup
ENST00000319516.8:c.752+15_752+19dup	ENSP00000316516.4:n.752+15_752+19dup
ENST00000379608.7:c.746+15_746+19dup	ENSP00000368928.3:n.746+15_746+19dup
ENST00000379613.7:c.770+15_770+19dup	ENSP00000368933.3:n.770+15_770+19dup
ENST00000461628.5:c.87+15_87+19dup
ENST00000466073.5:c.764+15_764+19dup	ENSP00000417495.1:n.764+15_764+19dup
ENST00000475264.5:c.478+15_478+19dup
ENST00000478375.5:n.764+15_764+19dup
ENST00000482890.5:c.764+15_764+19dup	ENSP00000418541.1:n.764+15_764+19dup
ENST00000488193.5:c.*261+15_*261+19dup	ENSP00000419823.1:n.*261+15_*261+19dup
ENST00000489805.5:c.*261+15_*261+19dup	ENSP00000420568.1:n.*261+15_*261+19dup
ENST00000497266.5:n.735+15_735+19dup
ENST00000498450.1:c.335+15_335+19dup	ENSP00000419961.1:n.335+15_335+19dup
NM_001032280.2:c.746+15_746+19dup	NP_001027451.1:n.746+15_746+19dup
NM_001042425.1:c.752+15_752+19dup	NP_001035890.1:n.752+15_752+19dup
NM_003220.2:c.764+15_764+19dup	NP_003211.1:n.764+15_764+19dup
XM_006715175.2:c.899+15_899+19dup	XP_006715238.1:n.899+15_899+19dup
XM_011514833.1:c.614+15_614+19dup	XP_011513135.1:n.614+15_614+19dup
XM_011514833.2:c.614+15_614+19dup	XP_011513135.1:n.614+15_614+19dup
XM_017011232.1:c.1010+15_1010+19dup	XP_016866721.1:n.1010+15_1010+19dup
NM_003220.3:c.764+15_764+19dup	NP_003211.1:n.764+15_764+19dup
NM_001032280.3:c.746+15_746+19dup	NP_001027451.1:n.746+15_746+19dup
NM_001042425.2:c.752+15_752+19dup	NP_001035890.1:n.752+15_752+19dup
NM_001372066.1:c.770+15_770+19dup MANE Select	NP_001358995.1:n.770+15_770+19dup
NM_001042425.3:c.752+15_752+19dup	NP_001035890.1:n.752+15_752+19dup