Canonical Allele Identifier: CA408317245

Gene: BFSP1

Linked Data

• MyVariant Identifiers: chr20:g.17479510T>A (hg19) ; chr20:g.17498865T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.17498865T>A , CM000682.2:g.17498865T>A	GRCh38
NC_000020.10:g.17479510T>A , CM000682.1:g.17479510T>A	GRCh37
NC_000020.9:g.17427510T>A	NCBI36
NG_012423.2:g.75356A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000377873.8:c.911A>T MANE Select	ENSP00000367104.3:p.Asn304Ile
ENST00000536626.7:c.494A>T	ENSP00000442522.1:p.Asn165Ile
ENST00000377868.6:c.536A>T	ENSP00000367099.2:p.Asn179Ile
ENST00000377873.7:c.911A>T	ENSP00000367104.3:p.Asn304Ile
ENST00000536626.5:c.494A>T	ENSP00000442522.1:p.Asn165Ile
NM_001161705.1:c.536A>T	NP_001155177.1:p.Asn179Ile
NM_001195.4:c.911A>T	NP_001186.1:p.Asn304Ile
NM_001278606.1:c.494A>T	NP_001265535.1:p.Asn165Ile
NM_001278607.1:c.578A>T	NP_001265536.1:p.Asn193Ile
NM_001278608.1:c.494A>T	NP_001265537.1:p.Asn165Ile
XM_011529312.1:c.494A>T	XP_011527614.1:p.Asn165Ile
XM_017028005.2:c.803A>T	XP_016883494.1:p.Asn268Ile
NM_001195.5:c.911A>T MANE Select	NP_001186.1:p.Asn304Ile
NM_001161705.2:c.536A>T	NP_001155177.1:p.Asn179Ile
NM_001278606.2:c.494A>T	NP_001265535.1:p.Asn165Ile
NM_001278607.2:c.578A>T	NP_001265536.1:p.Asn193Ile
NM_001278608.2:c.494A>T	NP_001265537.1:p.Asn165Ile