Canonical Allele Identifier: CA1584149879
Gene: SAR1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.134606928_134606929delinsCT , CM000667.2:g.134606928_134606929delinsCT GRCh38
NC_000005.9:g.133942618_133942619delinsCT , CM000667.1:g.133942618_133942619delinsCT GRCh37
NC_000005.8:g.133970517_133970518delinsCT NCBI36
NG_017002.1:g.30915_30916delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000402673.7:c.*21_*22delinsAG MANE Select ENSP00000385432.2:n.*21_*22delinsAG
ENST00000402673.6:c.*21_*22delinsAG ENSP00000385432.2:n.*21_*22delinsAG
ENST00000439578.5:c.*21_*22delinsAG ENSP00000404997.1:n.*21_*22delinsAG
ENST00000502539.5:c.*21_*22delinsAG ENSP00000426335.1:n.*21_*22delinsAG
ENST00000507419.5:c.*21_*22delinsAG ENSP00000425339.1:n.*21_*22delinsAG
ENST00000508363.5:n.2587_2588delinsAG
NM_001033503.2:c.*21_*22delinsAG NP_001028675.1:n.*21_*22delinsAG
NM_016103.3:c.*21_*22delinsAG NP_057187.1:n.*21_*22delinsAG
NM_016103.4:c.*21_*22delinsAG MANE Select NP_057187.1:n.*21_*22delinsAG
NM_001033503.3:c.*21_*22delinsAG NP_001028675.1:n.*21_*22delinsAG