Canonical Allele Identifier: CA360999643

Gene: SAR1B

Linked Data

• MyVariant Identifiers: chr5:g.133942717C>A (hg19) ; chr5:g.134607027C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134607027C>A , CM000667.2:g.134607027C>A	GRCh38
NC_000005.9:g.133942717C>A , CM000667.1:g.133942717C>A	GRCh37
NC_000005.8:g.133970616C>A	NCBI36
NG_017002.1:g.30817G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000402673.7:c.520G>T MANE Select	ENSP00000385432.2:p.Glu174Ter
ENST00000402673.6:c.520G>T	ENSP00000385432.2:p.Glu174Ter
ENST00000439578.5:c.520G>T	ENSP00000404997.1:p.Glu174Ter
ENST00000502539.5:c.316G>T	ENSP00000426335.1:p.Glu106Ter
ENST00000503318.5:c.*243G>T	ENSP00000425367.1:n.*243G>T
ENST00000507419.5:c.316G>T	ENSP00000425339.1:p.Glu106Ter
ENST00000508363.5:n.2489G>T
ENST00000509730.5:c.316G>T	ENSP00000423197.1:p.Glu106Ter
ENST00000509937.5:c.316G>T	ENSP00000424673.1:p.Glu106Ter
NM_001033503.2:c.520G>T	NP_001028675.1:p.Glu174Ter
NM_016103.3:c.520G>T	NP_057187.1:p.Glu174Ter
NM_016103.4:c.520G>T MANE Select	NP_057187.1:p.Glu174Ter
NM_001033503.3:c.520G>T	NP_001028675.1:p.Glu174Ter