Canonical Allele Identifier: CA3579007

Gene: MXD3

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177310463G>A , CM000667.2:g.177310463G>A	GRCh38
NC_000005.9:g.176737464G>A , CM000667.1:g.176737464G>A	GRCh37
NC_000005.8:g.176670070G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_031300.4:c.284C>T MANE Select	NP_112590.1:p.Thr95Met
ENST00000439742.7:c.284C>T MANE Select	ENSP00000401867.2:p.Thr95Met
NM_001142935.1:c.284C>T	NP_001136407.1:p.Thr95Met
NM_001142935.2:c.284C>T	NP_001136407.1:p.Thr95Met
NM_001394986.1:c.284C>T	NP_001381915.1:p.Thr95Met
NM_001394987.1:c.254C>T	NP_001381916.1:p.Thr85Met
NM_031300.3:c.284C>T	NP_112590.1:p.Thr95Met
ENST00000423571.6:c.284C>T	ENSP00000389716.2:p.Thr95Met
ENST00000427908.6:c.284C>T	ENSP00000416921.2:p.Thr95Met
ENST00000439742.6:c.284C>T	ENSP00000401867.2:p.Thr95Met
ENST00000502529.1:c.254C>T	ENSP00000425029.1:p.Thr85Met
ENST00000503473.5:n.1132C>T
ENST00000503782.1:n.1137C>T
ENST00000513063.5:c.284C>T	ENSP00000421463.1:p.Thr95Met
ENST00000513169.1:c.35C>T	ENSP00000427104.1:p.Thr12Met