Canonical Allele Identifier: CA2677252890

Gene: TFAP2A

Linked Data

• gnomAD v4: 6-10404478-CGGGGCGGGCG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.10404482_10404491del , CM000668.2:g.10404482_10404491del	GRCh38
NC_000006.11:g.10404715_10404724del , CM000668.1:g.10404715_10404724del	GRCh37
NC_000006.10:g.10512701_10512710del	NCBI36
NG_016151.1:g.20077_20086del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379608.9:c.746+20_746+29del	ENSP00000368928.3:n.746+20_746+29del
ENST00000379613.10:c.770+20_770+29del MANE Select	ENSP00000368933.5:n.770+20_770+29del
ENST00000482890.6:c.770+20_770+29del	ENSP00000418541.2:n.770+20_770+29del
ENST00000488193.7:c.*261+20_*261+29del	ENSP00000419823.3:n.*261+20_*261+29del
ENST00000498450.3:c.335+20_335+29del	ENSP00000419961.3:n.335+20_335+29del
ENST00000319516.8:c.752+20_752+29del	ENSP00000316516.4:n.752+20_752+29del
ENST00000379608.7:c.746+20_746+29del	ENSP00000368928.3:n.746+20_746+29del
ENST00000379613.7:c.770+20_770+29del	ENSP00000368933.3:n.770+20_770+29del
ENST00000461628.5:c.87+20_87+29del
ENST00000466073.5:c.764+20_764+29del	ENSP00000417495.1:n.764+20_764+29del
ENST00000475264.5:c.478+20_478+29del
ENST00000478375.5:n.764+20_764+29del
ENST00000482890.5:c.764+20_764+29del	ENSP00000418541.1:n.764+20_764+29del
ENST00000488193.5:c.*261+20_*261+29del	ENSP00000419823.1:n.*261+20_*261+29del
ENST00000489805.5:c.*261+20_*261+29del	ENSP00000420568.1:n.*261+20_*261+29del
ENST00000497266.5:n.735+20_735+29del
ENST00000498450.1:c.335+20_335+29del	ENSP00000419961.1:n.335+20_335+29del
NM_001032280.2:c.746+20_746+29del	NP_001027451.1:n.746+20_746+29del
NM_001042425.1:c.752+20_752+29del	NP_001035890.1:n.752+20_752+29del
NM_003220.2:c.764+20_764+29del	NP_003211.1:n.764+20_764+29del
XM_006715175.2:c.899+20_899+29del	XP_006715238.1:n.899+20_899+29del
XM_011514833.1:c.614+20_614+29del	XP_011513135.1:n.614+20_614+29del
XM_011514833.2:c.614+20_614+29del	XP_011513135.1:n.614+20_614+29del
XM_017011232.1:c.1010+20_1010+29del	XP_016866721.1:n.1010+20_1010+29del
NM_003220.3:c.764+20_764+29del	NP_003211.1:n.764+20_764+29del
NM_001032280.3:c.746+20_746+29del	NP_001027451.1:n.746+20_746+29del
NM_001042425.2:c.752+20_752+29del	NP_001035890.1:n.752+20_752+29del
NM_001372066.1:c.770+20_770+29del MANE Select	NP_001358995.1:n.770+20_770+29del
NM_001042425.3:c.752+20_752+29del	NP_001035890.1:n.752+20_752+29del