Canonical Allele Identifier: CA2771026900

Gene: TFAP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50830698_50830699insTTTTTT , CM000668.2:g.50830698_50830699insTTTTTT	GRCh38
NC_000006.11:g.50798411_50798412insTTTTTT , CM000668.1:g.50798411_50798412insTTTTTT	GRCh37
NC_000006.10:g.50906370_50906371insTTTTTT	NCBI36
NG_008438.1:g.16973_16974insTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.601+2019_601+2020insTTTTTT MANE Select	ENSP00000377265.2:n.601+2019_601+2020insTTTTTT
ENST00000393655.3:c.601+2019_601+2020insTTTTTT	ENSP00000377265.2:n.601+2019_601+2020insTTTTTT
NM_003221.3:c.601+2019_601+2020insTTTTTT	NP_003212.2:n.601+2019_601+2020insTTTTTT
XM_006715176.2:c.601+2019_601+2020insTTTTTT	XP_006715239.1:n.601+2019_601+2020insTTTTTT
XM_006715177.2:c.547+2019_547+2020insTTTTTT	XP_006715240.1:n.547+2019_547+2020insTTTTTT
XM_011514834.1:c.628+2019_628+2020insTTTTTT	XP_011513136.1:n.628+2019_628+2020insTTTTTT
XM_011514835.1:c.628+2019_628+2020insTTTTTT	XP_011513137.1:n.628+2019_628+2020insTTTTTT
XM_011514836.1:c.628+2019_628+2020insTTTTTT	XP_011513138.1:n.628+2019_628+2020insTTTTTT
XM_011514837.1:c.628+2019_628+2020insTTTTTT	XP_011513139.1:n.628+2019_628+2020insTTTTTT
XM_011514837.2:c.628+2019_628+2020insTTTTTT	XP_011513139.1:n.628+2019_628+2020insTTTTTT
XM_017011233.1:c.766+2019_766+2020insTTTTTT	XP_016866722.1:n.766+2019_766+2020insTTTTTT
XM_017011234.1:c.730+2019_730+2020insTTTTTT	XP_016866723.1:n.730+2019_730+2020insTTTTTT
XM_017011235.2:c.142+2019_142+2020insTTTTTT	XP_016866724.1:n.142+2019_142+2020insTTTTTT
NM_003221.4:c.601+2019_601+2020insTTTTTT MANE Select	NP_003212.2:n.601+2019_601+2020insTTTTTT