Canonical Allele Identifier: CA1882633895
Gene: SURF1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133352384_133352387delinsTAGG , CM000671.2:g.133352384_133352387delinsTAGG GRCh38
NC_000009.10:g.135209060_135209063delinsTAGG NCBI36
NG_008477.1:g.9120_9123delinsCCTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000371974.8:c.751+59_751+62delinsCCTA MANE Select ENSP00000361042.3:n.751+59_751+62delinsCCTA
ENST00000371974.7:c.751+59_751+62delinsCCTA ENSP00000361042.3:n.751+59_751+62delinsCCTA
ENST00000437995.1:n.661+59_661+62delinsCCTA
ENST00000495952.5:n.741+59_741+62delinsCCTA
ENST00000615505.4:c.424+59_424+62delinsCCTA ENSP00000482067.1:n.424+59_424+62delinsCCTA
NM_001280787.1:c.424+59_424+62delinsCCTA NP_001267716.1:n.424+59_424+62delinsCCTA
NM_003172.3:c.751+59_751+62delinsCCTA NP_003163.1:n.751+59_751+62delinsCCTA
XM_011518942.1:c.424+59_424+62delinsCCTA XP_011517244.1:n.424+59_424+62delinsCCTA
NM_003172.4:c.751+59_751+62delinsCCTA MANE Select NP_003163.1:n.751+59_751+62delinsCCTA