Canonical Allele Identifier: CA375693414
Gene: SURF1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr9:g.133351981A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133351981A>T , CM000671.2:g.133351981A>T GRCh38
NC_000009.10:g.135208657A>T NCBI36
NG_008477.1:g.9526T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000371974.8:c.835T>A MANE Select ENSP00000361042.3:p.Tyr279Asn
ENST00000371974.7:c.835T>A ENSP00000361042.3:p.Tyr279Asn
ENST00000437995.1:n.745T>A
ENST00000495952.5:n.825T>A
ENST00000615505.4:c.508T>A ENSP00000482067.1:p.Tyr170Asn
NM_001280787.1:c.508T>A NP_001267716.1:p.Tyr170Asn
NM_003172.3:c.835T>A NP_003163.1:p.Tyr279Asn
XM_011518942.1:c.508T>A XP_011517244.1:p.Tyr170Asn
NM_003172.4:c.835T>A MANE Select NP_003163.1:p.Tyr279Asn
Search 100 bp 5'
Search 100 bp 3'