Canonical Allele Identifier: CA7491310
Gene: NDUFAF1 HGNC NCBI

Linked Data

dbSNP Id: rs186056056

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.41396450G>C , CM000677.2:g.41396450G>C GRCh38
NC_000015.9:g.41688648G>C , CM000677.1:g.41688648G>C GRCh37
NC_000015.8:g.39475940G>C NCBI36
NG_031924.1:g.11011C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000260361.9:c.573+37C>G MANE Select ENSP00000260361.4:n.573+37C>G
ENST00000558719.2:c.573+37C>G ENSP00000454083.2:n.573+37C>G
ENST00000560978.2:c.573+37C>G ENSP00000453944.2:n.573+37C>G
ENST00000676533.1:c.573+37C>G ENSP00000504040.1:n.573+37C>G
ENST00000676906.1:c.114+37C>G ENSP00000503122.1:n.114+37C>G
ENST00000677477.1:n.1799+37C>G
ENST00000678029.1:c.573+37C>G ENSP00000503887.1:n.573+37C>G
ENST00000678745.1:c.573+37C>G ENSP00000503632.1:n.573+37C>G
ENST00000679094.1:c.573+37C>G ENSP00000504295.1:n.573+37C>G
ENST00000679240.1:n.971+37C>G
ENST00000260361.8:c.573+37C>G ENSP00000260361.4:n.573+37C>G
ENST00000559127.5:c.573+37C>G ENSP00000453027.1:n.573+37C>G
ENST00000560978.1:c.573+37C>G ENSP00000453944.1:n.573+37C>G
NM_016013.3:c.573+37C>G NP_057097.2:n.573+37C>G
NR_045620.1:n.971+37C>G
XM_006720555.1:c.573+37C>G XP_006720618.1:n.573+37C>G
XM_011521658.1:c.573+37C>G XP_011519960.1:n.573+37C>G
XM_011521659.1:c.573+37C>G XP_011519961.1:n.573+37C>G
XM_006720555.3:c.573+37C>G XP_006720618.1:n.573+37C>G
XM_011521659.3:c.573+37C>G XP_011519961.1:n.573+37C>G
XM_024449945.1:c.573+37C>G XP_024305713.1:n.573+37C>G
NM_016013.4:c.573+37C>G MANE Select NP_057097.2:n.573+37C>G
NR_045620.2:n.1007+37C>G