Canonical Allele Identifier: CA200832288
Gene: SURF1 HGNC NCBI

Linked Data

dbSNP Id: rs782064726 rs2130006688
gnomAD v4: 9-133352419-TC-T
MyVariant Identifiers: chr9:g.133352420del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133352421del , CM000671.2:g.133352421del GRCh38
NC_000009.10:g.135209097del NCBI36
NG_008477.1:g.9087del

Transcript Alleles

HGVS Amino-acid change
ENST00000371974.8:c.751+26del MANE Select ENSP00000361042.3:n.751+26del
ENST00000371974.7:c.751+26del ENSP00000361042.3:n.751+26del
ENST00000437995.1:n.661+26del
ENST00000495952.5:n.741+26del
ENST00000615505.4:c.424+26del ENSP00000482067.1:n.424+26del
NM_001280787.1:c.424+26del NP_001267716.1:n.424+26del
NM_003172.3:c.751+26del NP_003163.1:n.751+26del
XM_011518942.1:c.424+26del XP_011517244.1:n.424+26del
NM_003172.4:c.751+26del MANE Select NP_003163.1:n.751+26del
Search 100 bp 5'
Search 100 bp 3'