Canonical Allele Identifier: CA370406082
Community Standard Title: NM_004686.5(MTMR7):c.1966G>C (p.Val656Leu)
Gene: MTMR7 HGNC NCBI
VPS37A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.17299879C>G , CM000670.2:g.17299879C>G GRCh38
NC_000008.10:g.17157388C>G , CM000670.1:g.17157388C>G GRCh37
NC_000008.9:g.17201759C>G NCBI36
NG_032996.1:g.57988C>G
NG_032996.2:g.57988C>G

Transcript Alleles

HGVS Amino-acid Change
NM_004686.5:c.1966G>C (MTMR7) MANE Select NP_004677.3:p.Val656Leu
ENST00000180173.10:c.1966G>C (MTMR7) MANE Select ENSP00000180173.4:p.Val656Leu
NM_001363172.1:c.906+13452C>G (VPS37A) NP_001350101.1:n.906+13452C>G
NM_001363172.2:c.906+13452C>G (VPS37A) NP_001350101.1:n.906+13452C>G
NM_001363173.1:c.1194+13452C>G (VPS37A) NP_001350102.1:n.1194+13452C>G
NM_001363173.2:c.1194+13452C>G (VPS37A) NP_001350102.1:n.1194+13452C>G
NM_004686.4:c.1966G>C (MTMR7) NP_004677.3:p.Val656Leu
ENST00000180173.9:c.1966G>C (MTMR7) ENSP00000180173.4:p.Val656Leu
ENST00000519515.1:n.52+1721C>G (VPS37A)
ENST00000520997.1:n.224C>G (VPS37A)
ENST00000521162.5:n.566C>G (VPS37A)
XM_006716414.2:c.1255G>C (MTMR7) XP_006716477.2:p.Val419Leu
XM_006716414.3:c.1255G>C (MTMR7) XP_006716477.2:p.Val419Leu
XM_011544691.1:c.1984G>C (MTMR7) XP_011542993.1:p.Val662Leu
XM_011544692.1:c.1303G>C (MTMR7) XP_011542994.1:p.Val435Leu
XM_011544693.1:c.1255G>C (MTMR7) XP_011542995.1:p.Val419Leu
XM_011544693.2:c.1255G>C (MTMR7) XP_011542995.1:p.Val419Leu
XM_017013021.2:c.*1813C>G (VPS37A) XP_016868510.1:n.*1813C>G
XM_017013956.2:c.1102G>C (MTMR7) XP_016869445.1:p.Val368Leu
XM_024447325.1:c.1303G>C (MTMR7) XP_024303093.1:p.Val435Leu