Canonical Allele Identifier: CA10624338

Gene: TFAP2B

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50847607_50847608del , CM000668.2:g.50847607_50847608del	GRCh38
NC_000006.11:g.50815320_50815321del , CM000668.1:g.50815320_50815321del	GRCh37
NC_000006.10:g.50923279_50923280del	NCBI36
NG_008438.1:g.33882_33883del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.*4215_*4216del MANE Select	ENSP00000377265.2:n.*4215_*4216del
ENST00000393655.3:c.*4215_*4216del	ENSP00000377265.2:n.*4215_*4216del
NM_003221.3:c.*4215_*4216del	NP_003212.2:n.*4215_*4216del
XM_006715176.2:c.*3154_*3155del	XP_006715239.1:n.*3154_*3155del
XM_006715177.2:c.*3154_*3155del	XP_006715240.1:n.*3154_*3155del
XM_011514834.1:c.*3154_*3155del	XP_011513136.1:n.*3154_*3155del
XM_011514835.1:c.*3154_*3155del	XP_011513137.1:n.*3154_*3155del
XM_011514836.1:c.*1908_*1909del	XP_011513138.1:n.*1908_*1909del
XM_011514837.1:c.*4215_*4216del	XP_011513139.1:n.*4215_*4216del
XM_011514837.2:c.*4215_*4216del	XP_011513139.1:n.*4215_*4216del
XM_017011233.1:c.*4215_*4216del	XP_016866722.1:n.*4215_*4216del
XM_017011234.1:c.*4215_*4216del	XP_016866723.1:n.*4215_*4216del
XM_017011235.2:c.*4215_*4216del	XP_016866724.1:n.*4215_*4216del
NM_003221.4:c.*4215_*4216del MANE Select	NP_003212.2:n.*4215_*4216del