Canonical Allele Identifier: CA2353084879

Gene: BFSP1

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.17498972G= , CM000682.2:g.17498972G=	GRCh38
NC_000020.10:g.17479617G= , CM000682.1:g.17479617G=	GRCh37
NC_000020.9:g.17427617G=	NCBI36
NG_012423.2:g.75249C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000377873.8:c.804C= MANE Select	ENSP00000367104.3:p.Asn268=
ENST00000536626.7:c.387C=	ENSP00000442522.1:p.Asn129=
ENST00000377868.6:c.429C=	ENSP00000367099.2:p.Asn143=
ENST00000377873.7:c.804C=	ENSP00000367104.3:p.Asn268=
ENST00000536626.5:c.387C=	ENSP00000442522.1:p.Asn129=
NM_001161705.1:c.429C=	NP_001155177.1:p.Asn143=
NM_001195.4:c.804C=	NP_001186.1:p.Asn268=
NM_001278606.1:c.387C=	NP_001265535.1:p.Asn129=
NM_001278607.1:c.471C=	NP_001265536.1:p.Asn157=
NM_001278608.1:c.387C=	NP_001265537.1:p.Asn129=
XM_011529312.1:c.387C=	XP_011527614.1:p.Asn129=
XM_017028005.2:c.696C=	XP_016883494.1:p.Asn232=
NM_001195.5:c.804C= MANE Select	NP_001186.1:p.Asn268=
NM_001161705.2:c.429C=	NP_001155177.1:p.Asn143=
NM_001278606.2:c.387C=	NP_001265535.1:p.Asn129=
NM_001278607.2:c.471C=	NP_001265536.1:p.Asn157=
NM_001278608.2:c.387C=	NP_001265537.1:p.Asn129=