Canonical Allele Identifier: CA4643831
Community Standard Title: NM_004686.5(MTMR7):c.1516C>T (p.Arg506Cys)
Gene: MTMR7 HGNC NCBI
VPS37A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.17302258G>A , CM000670.2:g.17302258G>A GRCh38
NC_000008.10:g.17159767G>A , CM000670.1:g.17159767G>A GRCh37
NC_000008.9:g.17204138G>A NCBI36
NG_032996.2:g.60367G>A

Transcript Alleles

HGVS Amino-acid Change
NM_004686.5:c.1516C>T (MTMR7) MANE Select NP_004677.3:p.Arg506Cys
ENST00000180173.10:c.1516C>T (MTMR7) MANE Select ENSP00000180173.4:p.Arg506Cys
NM_001363172.1:c.906+15831G>A (VPS37A) NP_001350101.1:n.906+15831G>A
NM_001363172.2:c.906+15831G>A (VPS37A) NP_001350101.1:n.906+15831G>A
NM_001363173.1:c.1194+15831G>A (VPS37A) NP_001350102.1:n.1194+15831G>A
NM_001363173.2:c.1194+15831G>A (VPS37A) NP_001350102.1:n.1194+15831G>A
NM_004686.4:c.1516C>T (MTMR7) NP_004677.3:p.Arg506Cys
ENST00000180173.9:c.1516C>T (MTMR7) ENSP00000180173.4:p.Arg506Cys
ENST00000519515.1:n.97G>A (VPS37A)
ENST00000519590.5:n.528C>T (MTMR7)
ENST00000521857.5:c.1516C>T (MTMR7) ENSP00000429733.1:p.Arg506Cys
XM_006716414.2:c.805C>T (MTMR7) XP_006716477.2:p.Arg269Cys
XM_006716414.3:c.805C>T (MTMR7) XP_006716477.2:p.Arg269Cys
XM_011544691.1:c.1534C>T (MTMR7) XP_011542993.1:p.Arg512Cys
XM_011544692.1:c.853C>T (MTMR7) XP_011542994.1:p.Arg285Cys
XM_011544693.1:c.805C>T (MTMR7) XP_011542995.1:p.Arg269Cys
XM_011544693.2:c.805C>T (MTMR7) XP_011542995.1:p.Arg269Cys
XM_017013956.2:c.652C>T (MTMR7) XP_016869445.1:p.Arg218Cys
XM_024447325.1:c.853C>T (MTMR7) XP_024303093.1:p.Arg285Cys