Canonical Allele Identifier: CA375694228
Gene: SURF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.133353801A>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133353801A>C , CM000671.2:g.133353801A>C GRCh38
NC_000009.10:g.135210477A>C NCBI36
NG_008477.1:g.7706T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000371974.8:c.463T>G MANE Select ENSP00000361042.3:p.Ser155Ala
ENST00000371974.7:c.463T>G ENSP00000361042.3:p.Ser155Ala
ENST00000437995.1:n.409T>G
ENST00000495952.5:n.453T>G
ENST00000615505.4:c.136T>G ENSP00000482067.1:p.Ser46Ala
NM_001280787.1:c.136T>G NP_001267716.1:p.Ser46Ala
NM_003172.3:c.463T>G NP_003163.1:p.Ser155Ala
XM_011518942.1:c.136T>G XP_011517244.1:p.Ser46Ala
NM_003172.4:c.463T>G MANE Select NP_003163.1:p.Ser155Ala