Canonical Allele Identifier: CA2721291108

Gene: MALRD1

Linked Data

• dbSNP Id: rs2130928484

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.19425638C>T , CM000672.2:g.19425638C>T	GRCh38
NC_000010.10:g.19714567C>T , CM000672.1:g.19714567C>T	GRCh37
NC_000010.9:g.19754573C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000454679.7:c.4846-24669C>T MANE Select	ENSP00000412763.3:n.4846-24669C>T
ENST00000377266.7:c.2952+36029C>T	ENSP00000366477.3:n.2952+36029C>T
ENST00000441070.1:c.535-24669C>T	ENSP00000404330.1:n.535-24669C>T
ENST00000454679.6:c.4846-24669C>T	ENSP00000412763.3:n.4846-24669C>T
NM_001142308.2:c.4846-24669C>T	NP_001135780.2:n.4846-24669C>T
XM_011519453.1:c.4906-24669C>T	XP_011517755.1:n.4906-24669C>T
XM_011519454.1:c.4825-24669C>T	XP_011517756.1:n.4825-24669C>T
XM_011519455.1:c.4732-24669C>T	XP_011517757.1:n.4732-24669C>T
XM_011519453.2:c.4906-24669C>T	XP_011517755.1:n.4906-24669C>T
XM_011519455.2:c.4732-24669C>T	XP_011517757.1:n.4732-24669C>T
XM_017016182.1:c.4633-24669C>T	XP_016871671.1:n.4633-24669C>T
XM_017016183.1:c.4906-24669C>T	XP_016871672.1:n.4906-24669C>T
XM_017016184.1:c.3106-24669C>T	XP_016871673.1:n.3106-24669C>T
XM_017016185.1:c.3106-24669C>T	XP_016871674.1:n.3106-24669C>T
XM_017016186.1:c.1648-24669C>T	XP_016871675.1:n.1648-24669C>T
XR_001747102.1:n.5554-24669C>T
NM_001142308.3:c.4846-24669C>T MANE Select	NP_001135780.2:n.4846-24669C>T