Canonical Allele Identifier: CA1628079972

Gene: TFAP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50830779_50830780delinsGC , CM000668.2:g.50830779_50830780delinsGC	GRCh38
NC_000006.11:g.50798492_50798493delinsGC , CM000668.1:g.50798492_50798493delinsGC	GRCh37
NC_000006.10:g.50906451_50906452delinsGC	NCBI36
NG_008438.1:g.17054_17055delinsGC

Transcript Alleles

HGVS	Amino-acid change
ENST00000393655.4:c.601+2100_601+2101delinsGC MANE Select	ENSP00000377265.2:n.601+2100_601+2101deli...
ENST00000393655.3:c.601+2100_601+2101delinsGC	ENSP00000377265.2:n.601+2100_601+2101deli...
NM_003221.3:c.601+2100_601+2101delinsGC	NP_003212.2:n.601+2100_601+2101delinsGC
XM_006715176.2:c.601+2100_601+2101delinsGC	XP_006715239.1:n.601+2100_601+2101delinsG...
XM_006715177.2:c.547+2100_547+2101delinsGC	XP_006715240.1:n.547+2100_547+2101delinsG...
XM_011514834.1:c.628+2100_628+2101delinsGC	XP_011513136.1:n.628+2100_628+2101delinsG...
XM_011514835.1:c.628+2100_628+2101delinsGC	XP_011513137.1:n.628+2100_628+2101delinsG...
XM_011514836.1:c.628+2100_628+2101delinsGC	XP_011513138.1:n.628+2100_628+2101delinsG...
XM_011514837.1:c.628+2100_628+2101delinsGC	XP_011513139.1:n.628+2100_628+2101delinsG...
XM_011514837.2:c.628+2100_628+2101delinsGC	XP_011513139.1:n.628+2100_628+2101delinsG...
XM_017011233.1:c.766+2100_766+2101delinsGC	XP_016866722.1:n.766+2100_766+2101delinsG...
XM_017011234.1:c.730+2100_730+2101delinsGC	XP_016866723.1:n.730+2100_730+2101delinsG...
XM_017011235.2:c.142+2100_142+2101delinsGC	XP_016866724.1:n.142+2100_142+2101delinsG...
NM_003221.4:c.601+2100_601+2101delinsGC MANE Select	NP_003212.2:n.601+2100_601+2101delinsGC