Canonical Allele Identifier: CA361003309

Gene: SAR1B

Linked Data

• MyVariant Identifiers: chr5:g.133956625G>A (hg19) ; chr5:g.134620935G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.134620935G>A , CM000667.2:g.134620935G>A	GRCh38
NC_000005.9:g.133956625G>A , CM000667.1:g.133956625G>A	GRCh37
NC_000005.8:g.133984524G>A	NCBI36
NG_017002.1:g.16909C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000402673.7:c.176C>T MANE Select	ENSP00000385432.2:p.Pro59Leu
ENST00000402673.6:c.176C>T	ENSP00000385432.2:p.Pro59Leu
ENST00000439578.5:c.176C>T	ENSP00000404997.1:p.Pro59Leu
ENST00000502286.1:c.176C>T	ENSP00000423005.1:p.Pro59Leu
ENST00000503318.5:c.176C>T	ENSP00000425367.1:p.Pro59Leu
ENST00000505758.5:c.176C>T	ENSP00000425466.1:p.Pro59Leu
ENST00000507419.5:c.-151C>T	ENSP00000425339.1:n.-151C>T
NM_001033503.2:c.176C>T	NP_001028675.1:p.Pro59Leu
NM_016103.3:c.176C>T	NP_057187.1:p.Pro59Leu
NM_016103.4:c.176C>T MANE Select	NP_057187.1:p.Pro59Leu
NM_001033503.3:c.176C>T	NP_001028675.1:p.Pro59Leu