Canonical Allele Identifier: CA1584134947

Gene: SAR1B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134620933T= , CM000667.2:g.134620933T=	GRCh38
NC_000005.9:g.133956623T= , CM000667.1:g.133956623T=	GRCh37
NC_000005.8:g.133984522T=	NCBI36
NG_017002.1:g.16911A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000402673.7:c.178A= MANE Select	ENSP00000385432.2:p.Thr60=
ENST00000402673.6:c.178A=	ENSP00000385432.2:p.Thr60=
ENST00000439578.5:c.178A=	ENSP00000404997.1:p.Thr60=
ENST00000502286.1:c.178A=	ENSP00000423005.1:p.Thr60=
ENST00000503318.5:c.178A=	ENSP00000425367.1:p.Thr60=
ENST00000505758.5:c.178A=	ENSP00000425466.1:p.Thr60=
ENST00000507419.5:c.-149A=	ENSP00000425339.1:n.-149A=
NM_001033503.2:c.178A=	NP_001028675.1:p.Thr60=
NM_016103.3:c.178A=	NP_057187.1:p.Thr60=
NM_016103.4:c.178A= MANE Select	NP_057187.1:p.Thr60=
NM_001033503.3:c.178A=	NP_001028675.1:p.Thr60=