Canonical Allele Identifier: CA346098902
Community Standard Title: NM_145038.5(DRC1):c.391C>T (p.Gln131Ter)
Gene: DRC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26424305C>T , CM000664.2:g.26424305C>T GRCh38
NC_000002.11:g.26647173C>T , CM000664.1:g.26647173C>T GRCh37
NC_000002.10:g.26500677C>T NCBI36
NG_042824.1:g.27394C>T

Transcript Alleles

HGVS Amino-acid Change
NM_145038.5:c.391C>T MANE Select NP_659475.2:p.Gln131Ter
ENST00000288710.7:c.391C>T MANE Select ENSP00000288710.2:p.Gln131Ter
NM_145038.3:c.391C>T NP_659475.2:p.Gln131Ter
NM_145038.4:c.391C>T NP_659475.2:p.Gln131Ter
ENST00000288710.6:c.391C>T ENSP00000288710.2:p.Gln131Ter
ENST00000421869.5:c.356+2905C>T ENSP00000414375.1:n.356+2905C>T
ENST00000487307.5:n.247+2905C>T
ENST00000497651.1:n.281C>T
ENST00000649059.1:c.377C>T
XM_005264637.3:c.-79+2905C>T XP_005264694.1:n.-79+2905C>T
XM_005264638.3:c.-341+2905C>T XP_005264695.1:n.-341+2905C>T
XM_017005271.1:c.-490C>T XP_016860760.1:n.-490C>T
XM_024453218.1:c.-341+2905C>T XP_024308986.1:n.-341+2905C>T