Canonical Allele Identifier: CA375694221
Gene: SURF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.133353798T>A (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133353798T>A , CM000671.2:g.133353798T>A GRCh38
NC_000009.10:g.135210474T>A NCBI36
NG_008477.1:g.7709A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000371974.8:c.466A>T MANE Select ENSP00000361042.3:p.Thr156Ser
ENST00000371974.7:c.466A>T ENSP00000361042.3:p.Thr156Ser
ENST00000437995.1:n.412A>T
ENST00000495952.5:n.456A>T
ENST00000615505.4:c.139A>T ENSP00000482067.1:p.Thr47Ser
NM_001280787.1:c.139A>T NP_001267716.1:p.Thr47Ser
NM_003172.3:c.466A>T NP_003163.1:p.Thr156Ser
XM_011518942.1:c.139A>T XP_011517244.1:p.Thr47Ser
NM_003172.4:c.466A>T MANE Select NP_003163.1:p.Thr156Ser