Canonical Allele Identifier: CA375694196
Gene: SURF1 HGNC NCBI

Linked Data

gnomAD v4: 9-133353786-C-T
MyVariant Identifiers: chr9:g.133353786C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133353786C>T , CM000671.2:g.133353786C>T GRCh38
NC_000009.10:g.135210462C>T NCBI36
NG_008477.1:g.7721G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000371974.8:c.478G>A MANE Select ENSP00000361042.3:p.Ala160Thr
ENST00000371974.7:c.478G>A ENSP00000361042.3:p.Ala160Thr
ENST00000437995.1:n.424G>A
ENST00000495952.5:n.468G>A
ENST00000615505.4:c.151G>A ENSP00000482067.1:p.Ala51Thr
NM_001280787.1:c.151G>A NP_001267716.1:p.Ala51Thr
NM_003172.3:c.478G>A NP_003163.1:p.Ala160Thr
XM_011518942.1:c.151G>A XP_011517244.1:p.Ala51Thr
NM_003172.4:c.478G>A MANE Select NP_003163.1:p.Ala160Thr
Search 100 bp 5'
Search 100 bp 3'