Canonical Allele Identifier: CA1584149871

Gene: SAR1B

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134606918A= , CM000667.2:g.134606918A=	GRCh38
NC_000005.9:g.133942608A= , CM000667.1:g.133942608A=	GRCh37
NC_000005.8:g.133970507A=	NCBI36
NG_017002.1:g.30926T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000402673.7:c.*32T= MANE Select	ENSP00000385432.2:n.*32T=
ENST00000402673.6:c.*32T=	ENSP00000385432.2:n.*32T=
ENST00000439578.5:c.*32T=	ENSP00000404997.1:n.*32T=
ENST00000502539.5:c.*32T=	ENSP00000426335.1:n.*32T=
ENST00000507419.5:c.*32T=	ENSP00000425339.1:n.*32T=
ENST00000508363.5:n.2598T=
NM_001033503.2:c.*32T=	NP_001028675.1:n.*32T=
NM_016103.3:c.*32T=	NP_057187.1:n.*32T=
NM_016103.4:c.*32T= MANE Select	NP_057187.1:n.*32T=
NM_001033503.3:c.*32T=	NP_001028675.1:n.*32T=