Canonical Allele Identifier: CA2057673593
Gene: TMPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.98534326G= , CM000674.2:g.98534326G= GRCh38
NC_000012.11:g.98928104G= , CM000674.1:g.98928104G= GRCh37
NC_000012.10:g.97452235G= NCBI36
NG_021393.1:g.23754G= , LRG_443:g.23754G=

Transcript Alleles

HGVS Amino-acid change
ENST00000556029.6:c.565+2488G= MANE Select ENSP00000450627.1:n.565+2488G=
ENST00000261210.9:c.565+2488G= ENSP00000261210.5:n.565+2488G=
ENST00000266732.8:c.2069G= ENSP00000266732.4:p.Arg690=
ENST00000343315.9:c.565+2488G= ENSP00000340251.5:n.565+2488G=
ENST00000393053.6:c.565+2488G= ENSP00000376773.2:n.565+2488G=
ENST00000552831.1:n.643+2488G=
ENST00000556029.5:c.565+2488G= ENSP00000450627.1:n.565+2488G=
ENST00000556678.1:c.286+2488G= ENSP00000451552.1:n.286+2488G=
NM_001032283.2:c.565+2488G= , LRG_443t1:c.565+2488G= NP_001027454.1:n.565+2488G=
NM_001032284.2:c.565+2488G= NP_001027455.1:n.565+2488G=
NM_001307975.1:c.565+2488G= NP_001294904.1:n.565+2488G=
NM_003276.2:c.2069G= , LRG_443t2:c.2069G= NP_003267.1:p.Arg690=
XM_005269132.2:c.565+2488G= XP_005269189.1:n.565+2488G=
XM_005269132.4:c.565+2488G= XP_005269189.1:n.565+2488G=
XM_017019914.2:c.1163G= XP_016875403.1:p.Arg388=
NM_001032283.3:c.565+2488G= MANE Select NP_001027454.1:n.565+2488G=
NM_001032284.3:c.565+2488G= NP_001027455.1:n.565+2488G=
NM_001307975.2:c.565+2488G= NP_001294904.1:n.565+2488G=