Canonical Allele Identifier: CA1239812059
Gene: DRC1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.26444262A= , CM000664.2:g.26444262A= GRCh38
NC_000002.11:g.26667130A= , CM000664.1:g.26667130A= GRCh37
NC_000002.10:g.26520634A= NCBI36
NG_042824.1:g.47351A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000288710.7:c.1069A= MANE Select ENSP00000288710.2:p.Lys357=
ENST00000649059.1:c.915A=
ENST00000288710.6:c.1069A= ENSP00000288710.2:p.Lys357=
ENST00000421869.5:c.*382A= ENSP00000414375.1:n.*382A=
ENST00000483675.1:n.670A=
NM_145038.3:c.1069A= NP_659475.2:p.Lys357=
NM_145038.4:c.1069A= NP_659475.2:p.Lys357=
XM_005264637.3:c.451A= XP_005264694.1:p.Lys151=
XM_005264638.3:c.49A= XP_005264695.1:p.Lys17=
XM_017005271.1:c.49A= XP_016860760.1:p.Lys17=
XM_024453218.1:c.49A= XP_024308986.1:p.Lys17=
NM_145038.5:c.1069A= MANE Select NP_659475.2:p.Lys357=