Canonical Allele Identifier: CA1628080003

Gene: TFAP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50830793_50830794delinsAC , CM000668.2:g.50830793_50830794delinsAC	GRCh38
NC_000006.11:g.50798506_50798507delinsAC , CM000668.1:g.50798506_50798507delinsAC	GRCh37
NC_000006.10:g.50906465_50906466delinsAC	NCBI36
NG_008438.1:g.17068_17069delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.601+2114_601+2115delinsAC MANE Select	ENSP00000377265.2:n.601+2114_601+2115delinsAC
ENST00000393655.3:c.601+2114_601+2115delinsAC	ENSP00000377265.2:n.601+2114_601+2115delinsAC
NM_003221.3:c.601+2114_601+2115delinsAC	NP_003212.2:n.601+2114_601+2115delinsAC
XM_006715176.2:c.601+2114_601+2115delinsAC	XP_006715239.1:n.601+2114_601+2115delinsAC
XM_006715177.2:c.547+2114_547+2115delinsAC	XP_006715240.1:n.547+2114_547+2115delinsAC
XM_011514834.1:c.628+2114_628+2115delinsAC	XP_011513136.1:n.628+2114_628+2115delinsAC
XM_011514835.1:c.628+2114_628+2115delinsAC	XP_011513137.1:n.628+2114_628+2115delinsAC
XM_011514836.1:c.628+2114_628+2115delinsAC	XP_011513138.1:n.628+2114_628+2115delinsAC
XM_011514837.1:c.628+2114_628+2115delinsAC	XP_011513139.1:n.628+2114_628+2115delinsAC
XM_011514837.2:c.628+2114_628+2115delinsAC	XP_011513139.1:n.628+2114_628+2115delinsAC
XM_017011233.1:c.766+2114_766+2115delinsAC	XP_016866722.1:n.766+2114_766+2115delinsAC
XM_017011234.1:c.730+2114_730+2115delinsAC	XP_016866723.1:n.730+2114_730+2115delinsAC
XM_017011235.2:c.142+2114_142+2115delinsAC	XP_016866724.1:n.142+2114_142+2115delinsAC
NM_003221.4:c.601+2114_601+2115delinsAC MANE Select	NP_003212.2:n.601+2114_601+2115delinsAC