Canonical Allele Identifier: CA1584134939

Gene: SAR1B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134620916T= , CM000667.2:g.134620916T=	GRCh38
NC_000005.9:g.133956606T= , CM000667.1:g.133956606T=	GRCh37
NC_000005.8:g.133984505T=	NCBI36
NG_017002.1:g.16928A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000402673.7:c.178+17A= MANE Select	ENSP00000385432.2:n.178+17A=
ENST00000402673.6:c.178+17A=	ENSP00000385432.2:n.178+17A=
ENST00000439578.5:c.178+17A=	ENSP00000404997.1:n.178+17A=
ENST00000502286.1:c.178+17A=	ENSP00000423005.1:n.178+17A=
ENST00000503318.5:c.178+17A=	ENSP00000425367.1:n.178+17A=
ENST00000505758.5:c.178+17A=	ENSP00000425466.1:n.178+17A=
ENST00000507419.5:c.-149+17A=	ENSP00000425339.1:n.-149+17A=
NM_001033503.2:c.178+17A=	NP_001028675.1:n.178+17A=
NM_016103.3:c.178+17A=	NP_057187.1:n.178+17A=
NM_016103.4:c.178+17A= MANE Select	NP_057187.1:n.178+17A=
NM_001033503.3:c.178+17A=	NP_001028675.1:n.178+17A=