Canonical Allele Identifier: CA2645834163

Gene: BSND

Linked Data

• gnomAD v4: 1-54999053-GCTCTCCCTTGAAGCCTTGAGTTGCAGCGATTTCAGTGTCTT-G

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54999062_54999102del , CM000663.2:g.54999062_54999102del	GRCh38
NC_000001.10:g.55464735_55464775del , CM000663.1:g.55464735_55464775del	GRCh37
NC_000001.9:g.55237323_55237363del	NCBI36
NG_008965.1:g.5119_5159del
NG_008965.2:g.5130_5170del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651561.1:c.-125_-85del MANE Select	ENSP00000498282.1:n.-125_-85del
ENST00000371265.4:c.-125_-85del	ENSP00000360312.4:n.-125_-85del
NM_057176.2:c.-125_-85del	NP_476517.1:n.-125_-85del
NM_057176.3:c.-125_-85del MANE Select	NP_476517.1:n.-125_-85del