Canonical Allele Identifier: CA359158699

Gene: MTRR

Linked Data

• COSMIC: COSM3618081
• MyVariant Identifiers: chr5:g.7891493C>T (hg19) ; chr5:g.7891380C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7891380C>T , CM000667.2:g.7891380C>T	GRCh38
NC_000005.9:g.7891493C>T , CM000667.1:g.7891493C>T	GRCh37
NC_000005.8:g.7944493C>T	NCBI36
NG_008856.1:g.27277C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440940.7:c.1336C>T MANE Select	ENSP00000402510.2:p.Pro446Ser
ENST00000264668.6:c.1417C>T	ENSP00000264668.2:p.Pro473Ser
ENST00000440940.6:c.1336C>T	ENSP00000402510.2:p.Pro446Ser
ENST00000507202.1:n.12C>T
ENST00000507414.1:n.76C>T
ENST00000508101.5:n.576C>T
ENST00000510525.5:c.1272C>T
ENST00000511461.5:c.1249C>T
ENST00000512311.5:n.315C>T
ENST00000513439.5:c.*1043C>T	ENSP00000426710.1:n.*1043C>T
NM_002454.2:c.1336C>T	NP_002445.2:p.Pro446Ser
NM_024010.2:c.1417C>T	NP_076915.2:p.Pro473Ser
XM_011514043.1:c.1417C>T	XP_011512345.1:p.Pro473Ser
XM_011514044.1:c.1336C>T	XP_011512346.1:p.Pro446Ser
XR_241702.1:n.1350C>T
XR_241703.1:n.1343C>T
XR_925614.1:n.1462C>T
XR_925615.1:n.1614C>T
NM_001364440.1:c.1336C>T	NP_001351369.1:p.Pro446Ser
NM_001364441.1:c.1336C>T	NP_001351370.1:p.Pro446Ser
NM_001364442.1:c.1336C>T	NP_001351371.1:p.Pro446Ser
NM_024010.3:c.1336C>T	NP_076915.3:p.Pro446Ser
NR_134480.1:n.1459C>T
NR_134481.1:n.1384C>T
NR_134482.1:n.1319C>T
NR_157168.1:n.1389C>T
NR_157169.1:n.1249C>T
NR_157170.1:n.1415C>T
NR_157171.1:n.1272C>T
NR_157172.1:n.1186C>T
NR_157173.1:n.1426C>T
NR_157174.1:n.1427C>T
NR_157175.1:n.1581C>T
NR_157176.1:n.1744C>T
NR_157177.1:n.1424C>T
NR_157178.1:n.1452C>T
XM_024446063.1:c.1381C>T	XP_024301831.1:p.Pro461Ser
XM_024446064.1:c.1336C>T	XP_024301832.1:p.Pro446Ser
XR_001742071.1:n.1614C>T
XR_001742072.1:n.1591C>T
XR_001742074.1:n.1350C>T
XR_001742075.1:n.1502C>T
XR_001742076.1:n.1579C>T
XR_001742077.1:n.1602C>T
NM_001364440.2:c.1336C>T	NP_001351369.1:p.Pro446Ser
NM_001364441.2:c.1336C>T	NP_001351370.1:p.Pro446Ser
NM_001364442.2:c.1336C>T	NP_001351371.1:p.Pro446Ser
NM_002454.3:c.1336C>T MANE Select	NP_002445.2:p.Pro446Ser
NM_024010.4:c.1336C>T	NP_076915.3:p.Pro446Ser
NR_134480.2:n.1415C>T
NR_134481.2:n.1340C>T
NR_134482.2:n.1275C>T
NR_157168.2:n.1389C>T
NR_157169.2:n.1249C>T
NR_157170.2:n.1415C>T
NR_157171.2:n.1272C>T
NR_157172.2:n.1186C>T
NR_157173.2:n.1426C>T
NR_157174.2:n.1427C>T
NR_157175.2:n.1581C>T
NR_157176.2:n.1744C>T
NR_157177.2:n.1424C>T
NR_157178.2:n.1452C>T