Canonical Allele Identifier: CA1628080165

Gene: TFAP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50830966_50830967delinsAT , CM000668.2:g.50830966_50830967delinsAT	GRCh38
NC_000006.11:g.50798679_50798680delinsAT , CM000668.1:g.50798679_50798680delinsAT	GRCh37
NC_000006.10:g.50906638_50906639delinsAT	NCBI36
NG_008438.1:g.17241_17242delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.601+2287_601+2288delinsAT MANE Select	ENSP00000377265.2:n.601+2287_601+2288delinsAT
ENST00000393655.3:c.601+2287_601+2288delinsAT	ENSP00000377265.2:n.601+2287_601+2288delinsAT
NM_003221.3:c.601+2287_601+2288delinsAT	NP_003212.2:n.601+2287_601+2288delinsAT
XM_006715176.2:c.601+2287_601+2288delinsAT	XP_006715239.1:n.601+2287_601+2288delinsAT
XM_006715177.2:c.547+2287_547+2288delinsAT	XP_006715240.1:n.547+2287_547+2288delinsAT
XM_011514834.1:c.628+2287_628+2288delinsAT	XP_011513136.1:n.628+2287_628+2288delinsAT
XM_011514835.1:c.628+2287_628+2288delinsAT	XP_011513137.1:n.628+2287_628+2288delinsAT
XM_011514836.1:c.628+2287_628+2288delinsAT	XP_011513138.1:n.628+2287_628+2288delinsAT
XM_011514837.1:c.628+2287_628+2288delinsAT	XP_011513139.1:n.628+2287_628+2288delinsAT
XM_011514837.2:c.628+2287_628+2288delinsAT	XP_011513139.1:n.628+2287_628+2288delinsAT
XM_017011233.1:c.766+2287_766+2288delinsAT	XP_016866722.1:n.766+2287_766+2288delinsAT
XM_017011234.1:c.730+2287_730+2288delinsAT	XP_016866723.1:n.730+2287_730+2288delinsAT
XM_017011235.2:c.142+2287_142+2288delinsAT	XP_016866724.1:n.142+2287_142+2288delinsAT
NM_003221.4:c.601+2287_601+2288delinsAT MANE Select	NP_003212.2:n.601+2287_601+2288delinsAT