Canonical Allele Identifier: CA1717047202

Gene: BAZ1B

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.73442610_73442612delinsACT , CM000669.2:g.73442610_73442612delinsACT	GRCh38
NC_000007.13:g.72856940_72856942delinsACT , CM000669.1:g.72856940_72856942delinsACT	GRCh37
NC_000007.12:g.72494876_72494878delinsACT	NCBI36
NG_027679.1:g.84674_84676delinsAGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000339594.9:c.4095-59_4095-57delinsAGT MANE Select	ENSP00000342434.4:n.4095-59_4095-57delinsAGT
ENST00000339594.8:c.4095-59_4095-57delinsAGT	ENSP00000342434.4:n.4095-59_4095-57delinsAGT
ENST00000404251.1:c.4095-59_4095-57delinsAGT	ENSP00000385442.1:n.4095-59_4095-57delinsAGT
NM_032408.3:c.4095-59_4095-57delinsAGT	NP_115784.1:n.4095-59_4095-57delinsAGT
XM_017012773.2:c.4095-59_4095-57delinsAGT	XP_016868262.1:n.4095-59_4095-57delinsAGT
NM_032408.4:c.4095-59_4095-57delinsAGT MANE Select	NP_115784.1:n.4095-59_4095-57delinsAGT
NM_001370402.1:c.4095-59_4095-57delinsAGT	NP_001357331.1:n.4095-59_4095-57delinsAGT