Canonical Allele Identifier: CA375693867
Gene: SURF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.133352571A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133352571A>G , CM000671.2:g.133352571A>G GRCh38
NC_000009.10:g.135209247A>G NCBI36
NG_008477.1:g.8936T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000371974.8:c.626T>C MANE Select ENSP00000361042.3:p.Leu209Pro
ENST00000371974.7:c.626T>C ENSP00000361042.3:p.Leu209Pro
ENST00000437995.1:n.536T>C
ENST00000495952.5:n.616T>C
ENST00000615505.4:c.299T>C ENSP00000482067.1:p.Leu100Pro
NM_001280787.1:c.299T>C NP_001267716.1:p.Leu100Pro
NM_003172.3:c.626T>C NP_003163.1:p.Leu209Pro
XM_011518942.1:c.299T>C XP_011517244.1:p.Leu100Pro
NM_003172.4:c.626T>C MANE Select NP_003163.1:p.Leu209Pro
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