Canonical Allele Identifier: CA359157208

Gene: MTRR

Linked Data

• MyVariant Identifiers: chr5:g.7878317T>G (hg19) ; chr5:g.7878204T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7878204T>G , CM000667.2:g.7878204T>G	GRCh38
NC_000005.9:g.7878317T>G , CM000667.1:g.7878317T>G	GRCh37
NC_000005.8:g.7931317T>G	NCBI36
NG_008856.1:g.14101T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440940.7:c.662T>G MANE Select	ENSP00000402510.2:p.Ile221Ser
ENST00000264668.6:c.743T>G	ENSP00000264668.2:p.Ile248Ser
ENST00000440940.6:c.662T>G	ENSP00000402510.2:p.Ile221Ser
ENST00000510525.5:c.687T>G
ENST00000511461.5:c.575T>G
ENST00000513439.5:c.*369T>G	ENSP00000426710.1:n.*369T>G
ENST00000514220.5:c.447T>G
ENST00000514369.5:c.*326T>G	ENSP00000426132.1:n.*326T>G
NM_002454.2:c.662T>G	NP_002445.2:p.Ile221Ser
NM_024010.2:c.743T>G	NP_076915.2:p.Ile248Ser
XM_006714474.2:c.743T>G	XP_006714537.1:p.Ile248Ser
XM_011514043.1:c.743T>G	XP_011512345.1:p.Ile248Ser
XM_011514044.1:c.662T>G	XP_011512346.1:p.Ile221Ser
XM_011514045.1:c.743T>G	XP_011512347.1:p.Ile248Ser
XR_241702.1:n.765T>G
XR_241703.1:n.758T>G
XR_925614.1:n.765T>G
XR_925615.1:n.765T>G
NM_001364440.1:c.662T>G	NP_001351369.1:p.Ile221Ser
NM_001364441.1:c.662T>G	NP_001351370.1:p.Ile221Ser
NM_001364442.1:c.662T>G	NP_001351371.1:p.Ile221Ser
NM_024010.3:c.662T>G	NP_076915.3:p.Ile221Ser
NR_134480.1:n.785T>G
NR_134481.1:n.799T>G
NR_134482.1:n.645T>G
NR_157168.1:n.715T>G
NR_157169.1:n.575T>G
NR_157170.1:n.601T>G
NR_157171.1:n.575T>G
NR_157172.1:n.601T>G
NR_157173.1:n.729T>G
NR_157174.1:n.601T>G
NR_157175.1:n.755T>G
NR_157176.1:n.755T>G
NR_157177.1:n.750T>G
NR_157178.1:n.755T>G
XM_024446063.1:c.707T>G	XP_024301831.1:p.Ile236Ser
XM_024446064.1:c.662T>G	XP_024301832.1:p.Ile221Ser
XR_001742071.1:n.765T>G
XR_001742072.1:n.765T>G
XR_001742074.1:n.765T>G
XR_001742075.1:n.765T>G
XR_001742076.1:n.765T>G
XR_001742077.1:n.765T>G
NM_001364440.2:c.662T>G	NP_001351369.1:p.Ile221Ser
NM_001364441.2:c.662T>G	NP_001351370.1:p.Ile221Ser
NM_001364442.2:c.662T>G	NP_001351371.1:p.Ile221Ser
NM_002454.3:c.662T>G MANE Select	NP_002445.2:p.Ile221Ser
NM_024010.4:c.662T>G	NP_076915.3:p.Ile221Ser
NR_134480.2:n.741T>G
NR_134481.2:n.755T>G
NR_134482.2:n.601T>G
NR_157168.2:n.715T>G
NR_157169.2:n.575T>G
NR_157170.2:n.601T>G
NR_157171.2:n.575T>G
NR_157172.2:n.601T>G
NR_157173.2:n.729T>G
NR_157174.2:n.601T>G
NR_157175.2:n.755T>G
NR_157176.2:n.755T>G
NR_157177.2:n.750T>G
NR_157178.2:n.755T>G