Canonical Allele Identifier: CA375693717
Gene: SURF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.133352505T>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133352505T>A , CM000671.2:g.133352505T>A GRCh38
NC_000009.10:g.135209181T>A NCBI36
NG_008477.1:g.9002A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000371974.8:c.692A>T MANE Select ENSP00000361042.3:p.Asp231Val
ENST00000371974.7:c.692A>T ENSP00000361042.3:p.Asp231Val
ENST00000437995.1:n.602A>T
ENST00000495952.5:n.682A>T
ENST00000615505.4:c.365A>T ENSP00000482067.1:p.Asp122Val
NM_001280787.1:c.365A>T NP_001267716.1:p.Asp122Val
NM_003172.3:c.692A>T NP_003163.1:p.Asp231Val
XM_011518942.1:c.365A>T XP_011517244.1:p.Asp122Val
NM_003172.4:c.692A>T MANE Select NP_003163.1:p.Asp231Val