Canonical Allele Identifier: CA402983887
Gene: NDUFS7 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1388896T>A , CM000681.2:g.1388896T>A GRCh38
NC_000019.9:g.1388895T>A , CM000681.1:g.1388895T>A GRCh37
NC_000019.8:g.1339895T>A NCBI36
NG_008283.1:g.10013T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000233627.14:c.186T>A MANE Select ENSP00000233627.9:p.Tyr62Ter
ENST00000233627.13:c.186T>A ENSP00000233627.9:p.Tyr62Ter
ENST00000313408.11:c.186T>A ENSP00000364262.5:p.Tyr62Ter
ENST00000414651.3:c.276T>A ENSP00000406630.2:p.Tyr92Ter
ENST00000436115.6:n.209T>A
ENST00000534853.5:c.181T>A ENSP00000442822.1:p.Cys61Ser
ENST00000535382.1:n.438T>A
ENST00000538523.5:n.242T>A
ENST00000538662.5:n.213T>A
ENST00000538929.5:n.276T>A
ENST00000539480.5:c.186T>A ENSP00000443273.1:p.Tyr62Ter
ENST00000540530.5:n.177T>A
ENST00000543289.5:n.676T>A
ENST00000545446.5:n.477T>A
ENST00000546172.7:c.*182T>A ENSP00000467094.1:n.*182T>A
ENST00000546283.5:c.186T>A ENSP00000440348.1:p.Tyr62Ter
ENST00000618074.4:c.186T>A ENSP00000477895.1:p.Tyr62Ter
ENST00000620479.4:c.186T>A ENSP00000480984.1:p.Tyr62Ter
ENST00000622587.4:n.182T>A
NM_024407.4:c.186T>A NP_077718.3:p.Tyr62Ter
XM_005259556.3:c.186T>A XP_005259613.2:p.Tyr62Ter
NM_001363602.1:c.186T>A NP_001350531.1:p.Tyr62Ter
XM_017026768.2:c.186T>A XP_016882257.2:p.Tyr62Ter
XM_024451499.1:c.207T>A XP_024307267.1:p.Tyr69Ter
NM_024407.5:c.186T>A MANE Select NP_077718.3:p.Tyr62Ter
NM_001363602.2:c.186T>A NP_001350531.1:p.Tyr62Ter