Canonical Allele Identifier: CA1167959233

Gene: BSND

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.54999152_54999153delinsCG , CM000663.2:g.54999152_54999153delinsCG	GRCh38
NC_000001.10:g.55464825_55464826delinsCG , CM000663.1:g.55464825_55464826delinsCG	GRCh37
NC_000001.9:g.55237413_55237414delinsCG	NCBI36
NG_008965.1:g.5209_5210delinsCG
NG_008965.2:g.5220_5221delinsCG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000651561.1:c.-35_-34delinsCG MANE Select	ENSP00000498282.1:n.-35_-34delinsCG
ENST00000371265.4:c.-35_-34delinsCG	ENSP00000360312.4:n.-35_-34delinsCG
NM_057176.2:c.-35_-34delinsCG	NP_476517.1:n.-35_-34delinsCG
NM_057176.3:c.-35_-34delinsCG MANE Select	NP_476517.1:n.-35_-34delinsCG