Canonical Allele Identifier: CA443248008
Gene: MTRR HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.7878177C>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.7878064C>G , CM000667.2:g.7878064C>G GRCh38
NC_000005.9:g.7878177C>G , CM000667.1:g.7878177C>G GRCh37
NC_000005.8:g.7931177C>G NCBI36
NG_008856.1:g.13961C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000440940.7:c.522C>G MANE Select ENSP00000402510.2:p.Ser174=
ENST00000264668.6:c.603C>G ENSP00000264668.2:p.Ser201=
ENST00000440940.6:c.522C>G ENSP00000402510.2:p.Ser174=
ENST00000508890.1:n.335C>G
ENST00000510279.5:c.*191C>G ENSP00000427200.1:n.*191C>G
ENST00000510525.5:c.547C>G
ENST00000511461.5:c.435C>G
ENST00000513439.5:c.*229C>G ENSP00000426710.1:n.*229C>G
ENST00000514220.5:c.307C>G
ENST00000514369.5:c.*186C>G ENSP00000426132.1:n.*186C>G
NM_002454.2:c.522C>G NP_002445.2:p.Ser174=
NM_024010.2:c.603C>G NP_076915.2:p.Ser201=
XM_006714474.2:c.603C>G XP_006714537.1:p.Ser201=
XM_011514043.1:c.603C>G XP_011512345.1:p.Ser201=
XM_011514044.1:c.522C>G XP_011512346.1:p.Ser174=
XM_011514045.1:c.603C>G XP_011512347.1:p.Ser201=
XR_241702.1:n.625C>G
XR_241703.1:n.618C>G
XR_925614.1:n.625C>G
XR_925615.1:n.625C>G
NM_001364440.1:c.522C>G NP_001351369.1:p.Ser174=
NM_001364441.1:c.522C>G NP_001351370.1:p.Ser174=
NM_001364442.1:c.522C>G NP_001351371.1:p.Ser174=
NM_024010.3:c.522C>G NP_076915.3:p.Ser174=
NR_134480.1:n.645C>G
NR_134481.1:n.659C>G
NR_134482.1:n.505C>G
NR_157168.1:n.575C>G
NR_157169.1:n.435C>G
NR_157170.1:n.461C>G
NR_157171.1:n.435C>G
NR_157172.1:n.461C>G
NR_157173.1:n.589C>G
NR_157174.1:n.461C>G
NR_157175.1:n.615C>G
NR_157176.1:n.615C>G
NR_157177.1:n.610C>G
NR_157178.1:n.615C>G
XM_024446063.1:c.567C>G XP_024301831.1:p.Ser189=
XM_024446064.1:c.522C>G XP_024301832.1:p.Ser174=
XR_001742071.1:n.625C>G
XR_001742072.1:n.625C>G
XR_001742074.1:n.625C>G
XR_001742075.1:n.625C>G
XR_001742076.1:n.625C>G
XR_001742077.1:n.625C>G
NM_001364440.2:c.522C>G NP_001351369.1:p.Ser174=
NM_001364441.2:c.522C>G NP_001351370.1:p.Ser174=
NM_001364442.2:c.522C>G NP_001351371.1:p.Ser174=
NM_002454.3:c.522C>G MANE Select NP_002445.2:p.Ser174=
NM_024010.4:c.522C>G NP_076915.3:p.Ser174=
NR_134480.2:n.601C>G
NR_134481.2:n.615C>G
NR_134482.2:n.461C>G
NR_157168.2:n.575C>G
NR_157169.2:n.435C>G
NR_157170.2:n.461C>G
NR_157171.2:n.435C>G
NR_157172.2:n.461C>G
NR_157173.2:n.589C>G
NR_157174.2:n.461C>G
NR_157175.2:n.615C>G
NR_157176.2:n.615C>G
NR_157177.2:n.610C>G
NR_157178.2:n.615C>G