Canonical Allele Identifier: CA2317694133
Gene: NDUFS7 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1389832_1389836delinsTCCTG , CM000681.2:g.1389832_1389836delinsTCCTG GRCh38
NC_000019.9:g.1389831_1389835delinsTCCTG , CM000681.1:g.1389831_1389835delinsTCCTG GRCh37
NC_000019.8:g.1340831_1340835delinsTCCTG NCBI36
NG_008283.1:g.10949_10953delinsTCCTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000233627.14:c.228+894_228+898delinsTCCTG MANE Select ENSP00000233627.9:n.228+894_228+898delinsTCCTG
ENST00000233627.13:c.228+894_228+898delinsTCCTG ENSP00000233627.9:n.228+894_228+898delinsTCCTG
ENST00000313408.11:c.228+894_228+898delinsTCCTG ENSP00000364262.5:n.228+894_228+898delinsTCCTG
ENST00000414651.3:c.318+894_318+898delinsTCCTG ENSP00000406630.2:n.318+894_318+898delinsTCCTG
ENST00000436115.6:n.1145_1149delinsTCCTG
ENST00000534853.5:c.*22+894_*22+898delinsTCCTG ENSP00000442822.1:n.*22+894_*22+898delinsTCCTG
ENST00000535382.1:n.480+894_480+898delinsTCCTG
ENST00000538523.5:n.284+894_284+898delinsTCCTG
ENST00000538662.5:n.255+894_255+898delinsTCCTG
ENST00000538929.5:n.318+894_318+898delinsTCCTG
ENST00000539480.5:c.228+894_228+898delinsTCCTG ENSP00000443273.1:n.228+894_228+898delinsTCCTG
ENST00000540530.5:n.219+894_219+898delinsTCCTG
ENST00000543289.5:n.718+894_718+898delinsTCCTG
ENST00000545446.5:n.519+894_519+898delinsTCCTG
ENST00000546172.7:c.*224+894_*224+898delinsTCCTG ENSP00000467094.1:n.*224+894_*224+898delinsTCCTG
ENST00000546283.5:c.228+894_228+898delinsTCCTG ENSP00000440348.1:n.228+894_228+898delinsTCCTG
ENST00000618074.4:c.228+894_228+898delinsTCCTG ENSP00000477895.1:n.228+894_228+898delinsTCCTG
ENST00000620479.4:c.228+894_228+898delinsTCCTG ENSP00000480984.1:n.228+894_228+898delinsTCCTG
ENST00000622587.4:n.224+894_224+898delinsTCCTG
NM_024407.4:c.228+894_228+898delinsTCCTG NP_077718.3:n.228+894_228+898delinsTCCTG
XM_005259556.3:c.228+894_228+898delinsTCCTG XP_005259613.2:n.228+894_228+898delinsTCCTG
NM_001363602.1:c.228+894_228+898delinsTCCTG NP_001350531.1:n.228+894_228+898delinsTCCTG
XM_024451499.1:c.249+894_249+898delinsTCCTG XP_024307267.1:n.249+894_249+898delinsTCCTG
NM_024407.5:c.228+894_228+898delinsTCCTG MANE Select NP_077718.3:n.228+894_228+898delinsTCCTG
NM_001363602.2:c.228+894_228+898delinsTCCTG NP_001350531.1:n.228+894_228+898delinsTCCTG