Canonical Allele Identifier: CA918570825
Gene: SURF1 HGNC NCBI

Linked Data

dbSNP Id: rs1588689298

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.133352326_133352327insCCCCCCC , CM000671.2:g.133352326_133352327insCCCCCCC GRCh38
NC_000009.10:g.135209002_135209003insCCCCCCC NCBI36
NG_008477.1:g.9183_9184insGGGGGGG

Transcript Alleles

HGVS Amino-acid Change
ENST00000371974.8:c.751+122_751+123insGGGGGGG MANE Select ENSP00000361042.3:n.751+122_751+123insGGGGGGG
ENST00000371974.7:c.751+122_751+123insGGGGGGG ENSP00000361042.3:n.751+122_751+123insGGGGGGG
ENST00000437995.1:n.661+122_661+123insGGGGGGG
ENST00000495952.5:n.741+122_741+123insGGGGGGG
ENST00000615505.4:c.424+122_424+123insGGGGGGG ENSP00000482067.1:n.424+122_424+123insGGGGGGG
NM_001280787.1:c.424+122_424+123insGGGGGGG NP_001267716.1:n.424+122_424+123insGGGGGGG
NM_003172.3:c.751+122_751+123insGGGGGGG NP_003163.1:n.751+122_751+123insGGGGGGG
XM_011518942.1:c.424+122_424+123insGGGGGGG XP_011517244.1:n.424+122_424+123insGGGGGGG
NM_003172.4:c.751+122_751+123insGGGGGGG MANE Select NP_003163.1:n.751+122_751+123insGGGGGGG