Canonical Allele Identifier: CA2353084838

Gene: BFSP1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.17498878G= , CM000682.2:g.17498878G=	GRCh38
NC_000020.10:g.17479523G= , CM000682.1:g.17479523G=	GRCh37
NC_000020.9:g.17427523G=	NCBI36
NG_012423.2:g.75343C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000377873.8:c.898C= MANE Select	ENSP00000367104.3:p.Gln300=
ENST00000536626.7:c.481C=	ENSP00000442522.1:p.Gln161=
ENST00000377868.6:c.523C=	ENSP00000367099.2:p.Gln175=
ENST00000377873.7:c.898C=	ENSP00000367104.3:p.Gln300=
ENST00000536626.5:c.481C=	ENSP00000442522.1:p.Gln161=
NM_001161705.1:c.523C=	NP_001155177.1:p.Gln175=
NM_001195.4:c.898C=	NP_001186.1:p.Gln300=
NM_001278606.1:c.481C=	NP_001265535.1:p.Gln161=
NM_001278607.1:c.565C=	NP_001265536.1:p.Gln189=
NM_001278608.1:c.481C=	NP_001265537.1:p.Gln161=
XM_011529312.1:c.481C=	XP_011527614.1:p.Gln161=
XM_017028005.2:c.790C=	XP_016883494.1:p.Gln264=
NM_001195.5:c.898C= MANE Select	NP_001186.1:p.Gln300=
NM_001161705.2:c.523C=	NP_001155177.1:p.Gln175=
NM_001278606.2:c.481C=	NP_001265535.1:p.Gln161=
NM_001278607.2:c.565C=	NP_001265536.1:p.Gln189=
NM_001278608.2:c.481C=	NP_001265537.1:p.Gln161=