Canonical Allele Identifier: CA134820
Gene: TMPO HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 12707
dbSNP Id: rs17028450

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.98534325C>T , CM000674.2:g.98534325C>T GRCh38
NC_000012.11:g.98928103C>T , CM000674.1:g.98928103C>T GRCh37
NC_000012.10:g.97452234C>T NCBI36
NG_021393.1:g.23753C>T , LRG_443:g.23753C>T

Transcript Alleles

HGVS Amino-acid change
NM_001032283.2:c.565+2487C>T , LRG_443t1:c.565+2487C>T NP_001027454.1:p.=
NM_001032284.2:c.565+2487C>T VV NP_001027455.1:p.=
NM_001307975.1:c.565+2487C>T VV NP_001294904.1:p.=
NM_003276.2:c.2068C>T , LRG_443t2:c.2068C>T NP_003267.1:p.Arg690Cys
XM_005269132.2:c.565+2487C>T XP_005269189.1:p.=
XM_005269132.4:c.565+2487C>T
XM_017019914.2:c.1162C>T XP_016875403.1:p.Arg388Cys
ENST00000261210.9:c.565+2487C>T ENSP00000261210.5:p.=
ENST00000266732.8:c.2068C>T ENSP00000266732.4:p.Arg690Cys
ENST00000343315.9:c.565+2487C>T ENSP00000340251.5:p.=
ENST00000393053.6:c.565+2487C>T ENSP00000376773.2:p.=
ENST00000552831.1:n.643+2487C>T
ENST00000556029.5:c.565+2487C>T ENSP00000450627.1:p.=
ENST00000556678.1:n.286+2487C>T ENSP00000451552.1:p.=