Canonical Allele Identifier: CA72218608

Gene: OXSM

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.25790125T>G , CM000665.2:g.25790125T>G	GRCh38
NC_000003.11:g.25831616T>G , CM000665.1:g.25831616T>G	GRCh37
NC_000003.10:g.25806620T>G	NCBI36
NG_034108.1:g.4915A>C

Transcript Alleles

HGVS	Amino-acid Change
NM_017897.3:c.-54T>G MANE Select	NP_060367.1:n.-54T>G
ENST00000280701.8:c.-54T>G MANE Select	ENSP00000280701.3:n.-54T>G
NM_001145391.1:c.-54T>G	NP_001138863.1:n.-54T>G
NM_001145391.2:c.-54T>G	NP_001138863.1:n.-54T>G
NM_017897.2:c.-54T>G	NP_060367.1:n.-54T>G
NR_026937.1:n.54T>G
NR_026937.2:n.36T>G
ENST00000280701.7:c.-54T>G	ENSP00000280701.3:n.-54T>G
ENST00000420173.2:c.-54T>G	ENSP00000411303.2:n.-54T>G
ENST00000448177.1:c.-54T>G	ENSP00000404115.1:n.-54T>G
ENST00000452098.1:c.-31-865T>G	ENSP00000392334.1:n.-31-865T>G
XM_006713216.4:c.-723T>G	XP_006713279.1:n.-723T>G
XM_006713217.4:c.-1094T>G	XP_006713280.1:n.-1094T>G
XM_017006714.2:c.-1267T>G	XP_016862203.1:n.-1267T>G