Canonical Allele Identifier: CA1584134940

Gene: SAR1B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134620920G= , CM000667.2:g.134620920G=	GRCh38
NC_000005.9:g.133956610G= , CM000667.1:g.133956610G=	GRCh37
NC_000005.8:g.133984509G=	NCBI36
NG_017002.1:g.16924C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000402673.7:c.178+13C= MANE Select	ENSP00000385432.2:n.178+13C=
ENST00000402673.6:c.178+13C=	ENSP00000385432.2:n.178+13C=
ENST00000439578.5:c.178+13C=	ENSP00000404997.1:n.178+13C=
ENST00000502286.1:c.178+13C=	ENSP00000423005.1:n.178+13C=
ENST00000503318.5:c.178+13C=	ENSP00000425367.1:n.178+13C=
ENST00000505758.5:c.178+13C=	ENSP00000425466.1:n.178+13C=
ENST00000507419.5:c.-149+13C=	ENSP00000425339.1:n.-149+13C=
NM_001033503.2:c.178+13C=	NP_001028675.1:n.178+13C=
NM_016103.3:c.178+13C=	NP_057187.1:n.178+13C=
NM_016103.4:c.178+13C= MANE Select	NP_057187.1:n.178+13C=
NM_001033503.3:c.178+13C=	NP_001028675.1:n.178+13C=