Canonical Allele Identifier: CA1894659902
Gene: MALRD1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.19425550T= , CM000672.2:g.19425550T= GRCh38
NC_000010.10:g.19714479T= , CM000672.1:g.19714479T= GRCh37
NC_000010.9:g.19754485T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000454679.7:c.4846-24757T= MANE Select ENSP00000412763.3:n.4846-24757T=
ENST00000377266.7:c.2952+35941T= ENSP00000366477.3:n.2952+35941T=
ENST00000441070.1:c.535-24757T= ENSP00000404330.1:n.535-24757T=
ENST00000454679.6:c.4846-24757T= ENSP00000412763.3:n.4846-24757T=
NM_001142308.2:c.4846-24757T= NP_001135780.2:n.4846-24757T=
XM_011519453.1:c.4906-24757T= XP_011517755.1:n.4906-24757T=
XM_011519454.1:c.4825-24757T= XP_011517756.1:n.4825-24757T=
XM_011519455.1:c.4732-24757T= XP_011517757.1:n.4732-24757T=
XM_011519453.2:c.4906-24757T= XP_011517755.1:n.4906-24757T=
XM_011519455.2:c.4732-24757T= XP_011517757.1:n.4732-24757T=
XM_017016182.1:c.4633-24757T= XP_016871671.1:n.4633-24757T=
XM_017016183.1:c.4906-24757T= XP_016871672.1:n.4906-24757T=
XM_017016184.1:c.3106-24757T= XP_016871673.1:n.3106-24757T=
XM_017016185.1:c.3106-24757T= XP_016871674.1:n.3106-24757T=
XM_017016186.1:c.1648-24757T= XP_016871675.1:n.1648-24757T=
XR_001747102.1:n.5554-24757T=
NM_001142308.3:c.4846-24757T= MANE Select NP_001135780.2:n.4846-24757T=