Canonical Allele Identifier: CA2771023824

Gene: TFAP2B

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.50819114_50819115insC , CM000668.2:g.50819114_50819115insC	GRCh38
NC_000006.11:g.50786827_50786828insC , CM000668.1:g.50786827_50786828insC	GRCh37
NC_000006.10:g.50894786_50894787insC	NCBI36
NG_008438.1:g.5389_5390insC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000393655.4:c.81+142_81+143insC MANE Select	ENSP00000377265.2:n.81+142_81+143insC
ENST00000344788.7:c.48+142_48+143insC	ENSP00000342252.3:n.48+142_48+143insC
ENST00000393655.3:c.81+142_81+143insC	ENSP00000377265.2:n.81+142_81+143insC
NM_003221.3:c.81+142_81+143insC	NP_003212.2:n.81+142_81+143insC
XM_006715176.2:c.81+142_81+143insC	XP_006715239.1:n.81+142_81+143insC
XM_011514834.1:c.81+142_81+143insC	XP_011513136.1:n.81+142_81+143insC
XM_011514835.1:c.81+142_81+143insC	XP_011513137.1:n.81+142_81+143insC
XM_011514836.1:c.81+142_81+143insC	XP_011513138.1:n.81+142_81+143insC
XM_011514837.1:c.81+142_81+143insC	XP_011513139.1:n.81+142_81+143insC
XM_011514837.2:c.81+142_81+143insC	XP_011513139.1:n.81+142_81+143insC
XM_017011233.1:c.173+142_173+143insC	XP_016866722.1:n.173+142_173+143insC
XM_017011234.1:c.137+142_137+143insC	XP_016866723.1:n.137+142_137+143insC
XM_017011235.2:c.81+142_81+143insC	XP_016866724.1:n.81+142_81+143insC
NM_003221.4:c.81+142_81+143insC MANE Select	NP_003212.2:n.81+142_81+143insC