Canonical Allele Identifier: CA1584149862
Gene: SAR1B HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.134606912_134606913delinsGC , CM000667.2:g.134606912_134606913delinsGC GRCh38
NC_000005.9:g.133942602_133942603delinsGC , CM000667.1:g.133942602_133942603delinsGC GRCh37
NC_000005.8:g.133970501_133970502delinsGC NCBI36
NG_017002.1:g.30931_30932delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000402673.7:c.*37_*38delinsGC MANE Select ENSP00000385432.2:n.*37_*38delinsGC
ENST00000402673.6:c.*37_*38delinsGC ENSP00000385432.2:n.*37_*38delinsGC
ENST00000439578.5:c.*37_*38delinsGC ENSP00000404997.1:n.*37_*38delinsGC
ENST00000502539.5:c.*37_*38delinsGC ENSP00000426335.1:n.*37_*38delinsGC
ENST00000507419.5:c.*37_*38delinsGC ENSP00000425339.1:n.*37_*38delinsGC
ENST00000508363.5:n.2603_2604delinsGC
NM_001033503.2:c.*37_*38delinsGC NP_001028675.1:n.*37_*38delinsGC
NM_016103.3:c.*37_*38delinsGC NP_057187.1:n.*37_*38delinsGC
NM_016103.4:c.*37_*38delinsGC MANE Select NP_057187.1:n.*37_*38delinsGC
NM_001033503.3:c.*37_*38delinsGC NP_001028675.1:n.*37_*38delinsGC