Canonical Allele Identifier: CA2515996857

Gene: TFAP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50819221_50819222insAGAGCAGCGAAGT , CM000668.2:g.50819221_50819222insAGAGCAGCGAAGT	GRCh38
NC_000006.11:g.50786934_50786935insAGAGCAGCGAAGT , CM000668.1:g.50786934_50786935insAGAGCAGCGAAGT	GRCh37
NC_000006.10:g.50894893_50894894insAGAGCAGCGAAGT	NCBI36
NG_008438.1:g.5496_5497insAGAGCAGCGAAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.81+249_81+250insAGAGCAGCGAAGT MANE Select	ENSP00000377265.2:n.81+249_81+250insAGAGCAGCGAAGT
ENST00000344788.7:c.48+249_48+250insAGAGCAGCGAAGT	ENSP00000342252.3:n.48+249_48+250insAGAGCAGCGAAGT
ENST00000393655.3:c.81+249_81+250insAGAGCAGCGAAGT	ENSP00000377265.2:n.81+249_81+250insAGAGCAGCGAAGT
NM_003221.3:c.81+249_81+250insAGAGCAGCGAAGT	NP_003212.2:n.81+249_81+250insAGAGCAGCGAAGT
XM_006715176.2:c.81+249_81+250insAGAGCAGCGAAGT	XP_006715239.1:n.81+249_81+250insAGAGCAGCGAAGT
XM_011514834.1:c.81+249_81+250insAGAGCAGCGAAGT	XP_011513136.1:n.81+249_81+250insAGAGCAGCGAAGT
XM_011514835.1:c.81+249_81+250insAGAGCAGCGAAGT	XP_011513137.1:n.81+249_81+250insAGAGCAGCGAAGT
XM_011514836.1:c.81+249_81+250insAGAGCAGCGAAGT	XP_011513138.1:n.81+249_81+250insAGAGCAGCGAAGT
XM_011514837.1:c.81+249_81+250insAGAGCAGCGAAGT	XP_011513139.1:n.81+249_81+250insAGAGCAGCGAAGT
XM_011514837.2:c.81+249_81+250insAGAGCAGCGAAGT	XP_011513139.1:n.81+249_81+250insAGAGCAGCGAAGT
XM_017011233.1:c.173+249_173+250insAGAGCAGCGAAGT	XP_016866722.1:n.173+249_173+250insAGAGCAGCGAAGT
XM_017011234.1:c.137+249_137+250insAGAGCAGCGAAGT	XP_016866723.1:n.137+249_137+250insAGAGCAGCGAAGT
XM_017011235.2:c.81+249_81+250insAGAGCAGCGAAGT	XP_016866724.1:n.81+249_81+250insAGAGCAGCGAAGT
NM_003221.4:c.81+249_81+250insAGAGCAGCGAAGT MANE Select	NP_003212.2:n.81+249_81+250insAGAGCAGCGAAGT