Canonical Allele Identifier: CA402985971

Gene: NDUFS7

Linked Data

• MyVariant Identifiers: chr19:g.1391146A>C (hg19) ; chr19:g.1391147A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.1391147A>C , CM000681.2:g.1391147A>C	GRCh38
NC_000019.9:g.1391146A>C , CM000681.1:g.1391146A>C	GRCh37
NC_000019.8:g.1342146A>C	NCBI36
NG_008283.1:g.12264A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000233627.14:c.437A>C MANE Select	ENSP00000233627.9:p.Tyr146Ser
ENST00000233627.13:c.437A>C	ENSP00000233627.9:p.Tyr146Ser
ENST00000313408.11:c.437A>C	ENSP00000364262.5:p.Tyr146Ser
ENST00000414651.3:c.527A>C	ENSP00000406630.2:p.Tyr176Ser
ENST00000436115.6:n.2392A>C
ENST00000534853.5:c.*231A>C	ENSP00000442822.1:n.*231A>C
ENST00000535382.1:n.689A>C
ENST00000538523.5:n.493A>C
ENST00000538662.5:n.532A>C
ENST00000538929.5:n.527A>C
ENST00000539480.5:c.437A>C	ENSP00000443273.1:p.Tyr146Ser
ENST00000540530.5:n.428A>C
ENST00000543289.5:n.995A>C
ENST00000545446.5:n.728A>C
ENST00000546172.7:c.*433A>C	ENSP00000467094.1:n.*433A>C
ENST00000546283.5:c.437A>C	ENSP00000440348.1:p.Tyr146Ser
ENST00000618074.4:c.444A>C	ENSP00000477895.1:p.Leu148=
ENST00000620479.4:c.441A>C	ENSP00000480984.1:p.Leu147=
ENST00000622587.4:n.501A>C
NM_024407.4:c.437A>C	NP_077718.3:p.Tyr146Ser
XM_005259556.3:c.437A>C	XP_005259613.2:p.Tyr146Ser
NM_001363602.1:c.437A>C	NP_001350531.1:p.Tyr146Ser
XM_024451499.1:c.458A>C	XP_024307267.1:p.Tyr153Ser
NM_024407.5:c.437A>C MANE Select	NP_077718.3:p.Tyr146Ser
NM_001363602.2:c.437A>C	NP_001350531.1:p.Tyr146Ser