Canonical Allele Identifier: CA1914338919

Gene: ARID5B

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.61992026_61992028delinsCTG , CM000672.2:g.61992026_61992028delinsCTG	GRCh38
NC_000010.10:g.63751785_63751787delinsCTG , CM000672.1:g.63751785_63751787delinsCTG	GRCh37
NC_000010.9:g.63421791_63421793delinsCTG	NCBI36
NG_030027.1:g.95773_95775delinsCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000279873.12:c.503-8065_503-8063delinsCTG MANE Select	ENSP00000279873.7:n.503-8065_503-8063delinsCTG
ENST00000644638.1:c.503-8065_503-8063delinsCTG	ENSP00000494412.1:n.503-8065_503-8063delinsCTG
ENST00000681100.1:c.503-8065_503-8063delinsCTG	ENSP00000506119.1:n.503-8065_503-8063delinsCTG
ENST00000279873.11:c.503-8065_503-8063delinsCTG	ENSP00000279873.7:n.503-8065_503-8063delinsCTG
NM_032199.2:c.503-8065_503-8063delinsCTG	NP_115575.1:n.503-8065_503-8063delinsCTG
XM_011540262.1:c.502+51618_502+51620delinsCTG	XP_011538564.1:n.502+51618_502+51620delinsCTG
XM_024448230.1:c.-65-8065_-65-8063delinsCTG	XP_024303998.1:n.-65-8065_-65-8063delinsCTG
NM_032199.3:c.503-8065_503-8063delinsCTG MANE Select	NP_115575.1:n.503-8065_503-8063delinsCTG