Canonical Allele Identifier: CA1882633847
Gene: SURF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133352355_133352356delinsAG , CM000671.2:g.133352355_133352356delinsAG GRCh38
NC_000009.10:g.135209031_135209032delinsAG NCBI36
NG_008477.1:g.9151_9152delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000371974.8:c.751+90_751+91delinsCT MANE Select ENSP00000361042.3:n.751+90_751+91delinsCT
ENST00000371974.7:c.751+90_751+91delinsCT ENSP00000361042.3:n.751+90_751+91delinsCT
ENST00000437995.1:n.661+90_661+91delinsCT
ENST00000495952.5:n.741+90_741+91delinsCT
ENST00000615505.4:c.424+90_424+91delinsCT ENSP00000482067.1:n.424+90_424+91delinsCT
NM_001280787.1:c.424+90_424+91delinsCT NP_001267716.1:n.424+90_424+91delinsCT
NM_003172.3:c.751+90_751+91delinsCT NP_003163.1:n.751+90_751+91delinsCT
XM_011518942.1:c.424+90_424+91delinsCT XP_011517244.1:n.424+90_424+91delinsCT
NM_003172.4:c.751+90_751+91delinsCT MANE Select NP_003163.1:n.751+90_751+91delinsCT