Canonical Allele Identifier: CA2675321707
Gene: SAR1B HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.134606839dup , CM000667.2:g.134606839dup GRCh38
NC_000005.9:g.133942529dup , CM000667.1:g.133942529dup GRCh37
NC_000005.8:g.133970428dup NCBI36
NG_017002.1:g.31010dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000402673.7:c.*116dup MANE Select ENSP00000385432.2:n.*116dup
ENST00000402673.6:c.*116dup ENSP00000385432.2:n.*116dup
ENST00000439578.5:c.*116dup ENSP00000404997.1:n.*116dup
ENST00000502539.5:c.*116dup ENSP00000426335.1:n.*116dup
ENST00000507419.5:c.*116dup ENSP00000425339.1:n.*116dup
ENST00000508363.5:n.2682dup
NM_001033503.2:c.*116dup NP_001028675.1:n.*116dup
NM_016103.3:c.*116dup NP_057187.1:n.*116dup
NM_016103.4:c.*116dup MANE Select NP_057187.1:n.*116dup
NM_001033503.3:c.*116dup NP_001028675.1:n.*116dup