Canonical Allele Identifier: CA304059658

Gene: NDUFS7

Linked Data

• dbSNP Id: rs943689201
• MyVariant Identifiers: chr19:g.1391037A>C (hg19) ; chr19:g.1391038A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1391038A>C , CM000681.2:g.1391038A>C	GRCh38
NC_000019.9:g.1391037A>C , CM000681.1:g.1391037A>C	GRCh37
NC_000019.8:g.1342037A>C	NCBI36
NG_008283.1:g.12155A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000233627.14:c.396A>C MANE Select	ENSP00000233627.9:p.Pro132=
ENST00000233627.13:c.396A>C	ENSP00000233627.9:p.Pro132=
ENST00000313408.11:c.396A>C	ENSP00000364262.5:p.Pro132=
ENST00000414651.3:c.486A>C	ENSP00000406630.2:p.Pro162=
ENST00000436115.6:n.2351A>C
ENST00000534853.5:c.*190A>C	ENSP00000442822.1:n.*190A>C
ENST00000535382.1:n.648A>C
ENST00000538523.5:n.452A>C
ENST00000538662.5:n.423A>C
ENST00000538929.5:n.486A>C
ENST00000539480.5:c.396A>C	ENSP00000443273.1:p.Pro132=
ENST00000540530.5:n.387A>C
ENST00000543289.5:n.886A>C
ENST00000545446.5:n.687A>C
ENST00000546172.7:c.*392A>C	ENSP00000467094.1:n.*392A>C
ENST00000546283.5:c.396A>C	ENSP00000440348.1:p.Pro132=
ENST00000618074.4:c.396A>C	ENSP00000477895.1:p.Pro132=
ENST00000620479.4:c.396A>C	ENSP00000480984.1:p.Pro132=
ENST00000622587.4:n.392A>C
NM_024407.4:c.396A>C	NP_077718.3:p.Pro132=
XM_005259556.3:c.396A>C	XP_005259613.2:p.Pro132=
NM_001363602.1:c.396A>C	NP_001350531.1:p.Pro132=
XM_024451499.1:c.417A>C	XP_024307267.1:p.Pro139=
NM_024407.5:c.396A>C MANE Select	NP_077718.3:p.Pro132=
NM_001363602.2:c.396A>C	NP_001350531.1:p.Pro132=