Canonical Allele Identifier: CA1628079680

Gene: TFAP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50830563_50830564delinsCA , CM000668.2:g.50830563_50830564delinsCA	GRCh38
NC_000006.11:g.50798276_50798277delinsCA , CM000668.1:g.50798276_50798277delinsCA	GRCh37
NC_000006.10:g.50906235_50906236delinsCA	NCBI36
NG_008438.1:g.16838_16839delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.601+1884_601+1885delinsCA MANE Select	ENSP00000377265.2:n.601+1884_601+1885delinsCA
ENST00000393655.3:c.601+1884_601+1885delinsCA	ENSP00000377265.2:n.601+1884_601+1885delinsCA
NM_003221.3:c.601+1884_601+1885delinsCA	NP_003212.2:n.601+1884_601+1885delinsCA
XM_006715176.2:c.601+1884_601+1885delinsCA	XP_006715239.1:n.601+1884_601+1885delinsCA
XM_006715177.2:c.547+1884_547+1885delinsCA	XP_006715240.1:n.547+1884_547+1885delinsCA
XM_011514834.1:c.628+1884_628+1885delinsCA	XP_011513136.1:n.628+1884_628+1885delinsCA
XM_011514835.1:c.628+1884_628+1885delinsCA	XP_011513137.1:n.628+1884_628+1885delinsCA
XM_011514836.1:c.628+1884_628+1885delinsCA	XP_011513138.1:n.628+1884_628+1885delinsCA
XM_011514837.1:c.628+1884_628+1885delinsCA	XP_011513139.1:n.628+1884_628+1885delinsCA
XM_011514837.2:c.628+1884_628+1885delinsCA	XP_011513139.1:n.628+1884_628+1885delinsCA
XM_017011233.1:c.766+1884_766+1885delinsCA	XP_016866722.1:n.766+1884_766+1885delinsCA
XM_017011234.1:c.730+1884_730+1885delinsCA	XP_016866723.1:n.730+1884_730+1885delinsCA
XM_017011235.2:c.142+1884_142+1885delinsCA	XP_016866724.1:n.142+1884_142+1885delinsCA
NM_003221.4:c.601+1884_601+1885delinsCA MANE Select	NP_003212.2:n.601+1884_601+1885delinsCA