Canonical Allele Identifier: CA6961843

Gene: MTRF1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.41260637G>T , CM000675.2:g.41260637G>T	GRCh38
NC_000013.10:g.41834773G>T , CM000675.1:g.41834773G>T	GRCh37
NC_000013.9:g.40732773G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379480.9:c.271C>A MANE Select	ENSP00000368793.3:p.Gln91Lys
ENST00000239852.10:c.271C>A	ENSP00000481161.1:p.Gln91Lys
ENST00000379477.5:c.271C>A	ENSP00000368790.1:p.Gln91Lys
ENST00000379480.8:c.271C>A	ENSP00000368793.3:p.Gln91Lys
ENST00000430347.3:c.271C>A	ENSP00000400031.3:p.Gln91Lys
ENST00000452359.5:c.271C>A	ENSP00000399279.1:p.Gln91Lys
ENST00000497679.6:c.271C>A	ENSP00000484414.1:p.Gln91Lys
NM_004294.2:c.271C>A	NP_004285.2:p.Gln91Lys
XM_005266599.1:c.271C>A	XP_005266656.1:p.Gln91Lys
XM_006719897.1:c.271C>A	XP_006719960.1:p.Gln91Lys
XM_006719898.1:c.271C>A	XP_006719961.1:p.Gln91Lys
XM_006719900.1:c.271C>A	XP_006719963.1:p.Gln91Lys
XM_011535315.1:c.427C>A	XP_011533617.1:p.Gln143Lys
XM_011535316.1:c.427C>A	XP_011533618.1:p.Gln143Lys
XM_011535317.1:c.310C>A	XP_011533619.1:p.Gln104Lys
XM_011535318.1:c.271C>A	XP_011533620.1:p.Gln91Lys
XM_011535319.1:c.271C>A	XP_011533621.1:p.Gln91Lys
XM_011535320.1:c.271C>A	XP_011533622.1:p.Gln91Lys
XM_011535321.1:c.271C>A	XP_011533623.1:p.Gln91Lys
XM_011535322.1:c.271C>A	XP_011533624.1:p.Gln91Lys
XM_011535323.1:c.271C>A	XP_011533625.1:p.Gln91Lys
XM_011535324.1:c.271C>A	XP_011533626.1:p.Gln91Lys
XM_011535325.1:c.271C>A	XP_011533627.1:p.Gln91Lys
XM_011535326.1:c.427C>A	XP_011533628.1:p.Gln143Lys
XM_011535327.1:c.427C>A	XP_011533629.1:p.Gln143Lys
NM_001354073.1:c.271C>A	NP_001341002.1:p.Gln91Lys
NM_001354074.1:c.271C>A	NP_001341003.1:p.Gln91Lys
NM_001354076.1:c.271C>A	NP_001341005.1:p.Gln91Lys
NM_004294.3:c.271C>A	NP_004285.2:p.Gln91Lys
XM_006719898.2:c.271C>A	XP_006719961.1:p.Gln91Lys
XM_006719900.2:c.271C>A	XP_006719963.1:p.Gln91Lys
XM_011535315.2:c.427C>A	XP_011533617.1:p.Gln143Lys
XM_011535317.2:c.310C>A	XP_011533619.1:p.Gln104Lys
XM_011535318.3:c.271C>A	XP_011533620.1:p.Gln91Lys
XM_011535320.2:c.271C>A	XP_011533622.1:p.Gln91Lys
XM_011535321.2:c.271C>A	XP_011533623.1:p.Gln91Lys
XM_011535323.2:c.271C>A	XP_011533625.1:p.Gln91Lys
XM_011535325.2:c.271C>A	XP_011533627.1:p.Gln91Lys
XM_011535326.3:c.427C>A	XP_011533628.1:p.Gln143Lys
XM_011535327.2:c.427C>A	XP_011533629.1:p.Gln143Lys
XM_017020856.1:c.427C>A	XP_016876345.1:p.Gln143Lys
XM_017020857.1:c.427C>A	XP_016876346.1:p.Gln143Lys
XM_017020858.1:c.427C>A	XP_016876347.1:p.Gln143Lys
XM_017020859.2:c.427C>A	XP_016876348.1:p.Gln143Lys
XM_017020860.1:c.310C>A	XP_016876349.1:p.Gln104Lys
XM_017020861.2:c.310C>A	XP_016876350.1:p.Gln104Lys
XM_017020865.2:c.271C>A	XP_016876354.1:p.Gln91Lys
XM_017020866.2:c.271C>A	XP_016876355.1:p.Gln91Lys
XM_017020867.1:c.271C>A	XP_016876356.1:p.Gln91Lys
XM_017020868.1:c.271C>A	XP_016876357.1:p.Gln91Lys
XM_017020869.2:c.271C>A	XP_016876358.1:p.Gln91Lys
XM_017020870.2:c.271C>A	XP_016876359.1:p.Gln91Lys
XM_017020871.1:c.271C>A	XP_016876360.1:p.Gln91Lys
XM_017020872.1:c.427C>A	XP_016876361.1:p.Gln143Lys
XM_017020874.1:c.271C>A	XP_016876363.1:p.Gln91Lys
XM_017020875.1:c.271C>A	XP_016876364.1:p.Gln91Lys
XM_017020877.1:c.-346C>A	XP_016876366.1:n.-346C>A
XM_017020878.2:c.271C>A	XP_016876367.1:p.Gln91Lys
XM_017020879.2:c.271C>A	XP_016876368.1:p.Gln91Lys
XM_024449440.1:c.271C>A	XP_024305208.1:p.Gln91Lys
XM_024449441.1:c.271C>A	XP_024305209.1:p.Gln91Lys
XM_024449442.1:c.271C>A	XP_024305210.1:p.Gln91Lys
XM_024449443.1:c.271C>A	XP_024305211.1:p.Gln91Lys
XM_024449444.1:c.271C>A	XP_024305212.1:p.Gln91Lys
XR_001749741.1:n.369C>A
XR_001749742.2:n.1789C>A
XR_001749743.1:n.510C>A
XR_001749744.2:n.1787C>A
XR_002957484.1:n.1594C>A
NM_004294.4:c.271C>A MANE Select	NP_004285.2:p.Gln91Lys