Canonical Allele Identifier: CA860708659
Gene: SURF1 HGNC NCBI

Linked Data

dbSNP Id: rs1233475698
MyVariant Identifiers: chr9:g.133352957del (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133352960del , CM000671.2:g.133352960del GRCh38
NC_000009.10:g.135209636del NCBI36
NG_008477.1:g.8550del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371974.8:c.516-191del MANE Select ENSP00000361042.3:n.516-191del
ENST00000371974.7:c.516-191del ENSP00000361042.3:n.516-191del
ENST00000437995.1:n.462-227del
ENST00000495952.5:n.506-191del
ENST00000615505.4:c.189-191del ENSP00000482067.1:n.189-191del
NM_001280787.1:c.189-191del NP_001267716.1:n.189-191del
NM_003172.3:c.516-191del NP_003163.1:n.516-191del
XM_011518942.1:c.189-191del XP_011517244.1:n.189-191del
NM_003172.4:c.516-191del MANE Select NP_003163.1:n.516-191del