Canonical Allele Identifier: CA1882633922
Gene: SURF1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133352399T= , CM000671.2:g.133352399T= GRCh38
NC_000009.10:g.135209075T= NCBI36
NG_008477.1:g.9108A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000371974.8:c.751+47A= MANE Select ENSP00000361042.3:n.751+47A=
ENST00000371974.7:c.751+47A= ENSP00000361042.3:n.751+47A=
ENST00000437995.1:n.661+47A=
ENST00000495952.5:n.741+47A=
ENST00000615505.4:c.424+47A= ENSP00000482067.1:n.424+47A=
NM_001280787.1:c.424+47A= NP_001267716.1:n.424+47A=
NM_003172.3:c.751+47A= NP_003163.1:n.751+47A=
XM_011518942.1:c.424+47A= XP_011517244.1:n.424+47A=
NM_003172.4:c.751+47A= MANE Select NP_003163.1:n.751+47A=
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