Canonical Allele Identifier: CA3195771

Gene: MTRR

Linked Data

• ClinVar Variation Id: 1093581
• ClinVar RCV Id: RCV001413771
• dbSNP Id: rs770336060
• ExAC: 5:7885852 C / T
• gnomAD v2: 5-7885852-C-T
• gnomAD v3: 5-7885739-C-T
• gnomAD v4: 5-7885739-C-T
• MyVariant Identifiers: chr5:g.7885852C>T (hg19) ; chr5:g.7885739C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.7885739C>T , CM000667.2:g.7885739C>T	GRCh38
NC_000005.9:g.7885852C>T , CM000667.1:g.7885852C>T	GRCh37
NC_000005.8:g.7938852C>T	NCBI36
NG_008856.1:g.21636C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000440940.7:c.942C>T MANE Select	ENSP00000402510.2:p.Ser314=
ENST00000264668.6:c.1023C>T	ENSP00000264668.2:p.Ser341=
ENST00000440940.6:c.942C>T	ENSP00000402510.2:p.Ser314=
ENST00000508101.5:n.182C>T
ENST00000510525.5:c.967C>T
ENST00000511461.5:c.855C>T
ENST00000513439.5:c.*649C>T	ENSP00000426710.1:n.*649C>T
NM_002454.2:c.942C>T	NP_002445.2:p.Ser314=
NM_024010.2:c.1023C>T	NP_076915.2:p.Ser341=
XM_006714474.2:c.1023C>T	XP_006714537.1:p.Ser341=
XM_011514043.1:c.1023C>T	XP_011512345.1:p.Ser341=
XM_011514044.1:c.942C>T	XP_011512346.1:p.Ser314=
XM_011514045.1:c.1163C>T	XP_011512347.1:p.Ala388Val
XR_241702.1:n.1045C>T
XR_241703.1:n.1038C>T
XR_925614.1:n.1045C>T
XR_925615.1:n.1045C>T
NM_001364440.1:c.942C>T	NP_001351369.1:p.Ser314=
NM_001364441.1:c.942C>T	NP_001351370.1:p.Ser314=
NM_001364442.1:c.942C>T	NP_001351371.1:p.Ser314=
NM_024010.3:c.942C>T	NP_076915.3:p.Ser314=
NR_134480.1:n.1065C>T
NR_134481.1:n.1079C>T
NR_134482.1:n.925C>T
NR_157168.1:n.995C>T
NR_157169.1:n.855C>T
NR_157170.1:n.1021C>T
NR_157171.1:n.855C>T
NR_157172.1:n.881C>T
NR_157173.1:n.1009C>T
NR_157174.1:n.881C>T
NR_157175.1:n.1035C>T
NR_157176.1:n.1175C>T
NR_157177.1:n.1030C>T
NR_157178.1:n.1035C>T
XM_024446063.1:c.987C>T	XP_024301831.1:p.Ser329=
XM_024446064.1:c.942C>T	XP_024301832.1:p.Ser314=
XR_001742071.1:n.1045C>T
XR_001742072.1:n.1045C>T
XR_001742074.1:n.1045C>T
XR_001742075.1:n.1045C>T
XR_001742076.1:n.1185C>T
XR_001742077.1:n.1185C>T
NM_001364440.2:c.942C>T	NP_001351369.1:p.Ser314=
NM_001364441.2:c.942C>T	NP_001351370.1:p.Ser314=
NM_001364442.2:c.942C>T	NP_001351371.1:p.Ser314=
NM_002454.3:c.942C>T MANE Select	NP_002445.2:p.Ser314=
NM_024010.4:c.942C>T	NP_076915.3:p.Ser314=
NR_134480.2:n.1021C>T
NR_134481.2:n.1035C>T
NR_134482.2:n.881C>T
NR_157168.2:n.995C>T
NR_157169.2:n.855C>T
NR_157170.2:n.1021C>T
NR_157171.2:n.855C>T
NR_157172.2:n.881C>T
NR_157173.2:n.1009C>T
NR_157174.2:n.881C>T
NR_157175.2:n.1035C>T
NR_157176.2:n.1175C>T
NR_157177.2:n.1030C>T
NR_157178.2:n.1035C>T