Canonical Allele Identifier: CA6732304
Community Standard Title: NM_001032283.3(TMPO):c.565+1287A>G
Gene: TMPO HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.98533125A>G , CM000674.2:g.98533125A>G GRCh38
NC_000012.11:g.98926903A>G , CM000674.1:g.98926903A>G GRCh37
NC_000012.10:g.97451034A>G NCBI36
NG_021393.1:g.22553A>G , LRG_443:g.22553A>G

Transcript Alleles

HGVS Amino-acid Change
NM_001032283.3:c.565+1287A>G MANE Select NP_001027454.1:n.565+1287A>G
ENST00000556029.6:c.565+1287A>G MANE Select ENSP00000450627.1:n.565+1287A>G
NM_001032283.2:c.565+1287A>G , LRG_443t1:c.565+1287A>G NP_001027454.1:n.565+1287A>G
NM_001032284.2:c.565+1287A>G NP_001027455.1:n.565+1287A>G
NM_001032284.3:c.565+1287A>G NP_001027455.1:n.565+1287A>G
NM_001307975.1:c.565+1287A>G NP_001294904.1:n.565+1287A>G
NM_001307975.2:c.565+1287A>G NP_001294904.1:n.565+1287A>G
NM_003276.2:c.868A>G , LRG_443t2:c.868A>G NP_003267.1:p.Lys290Glu
ENST00000261210.9:c.565+1287A>G ENSP00000261210.5:n.565+1287A>G
ENST00000266732.8:c.868A>G ENSP00000266732.4:p.Lys290Glu
ENST00000343315.9:c.565+1287A>G ENSP00000340251.5:n.565+1287A>G
ENST00000393053.6:c.565+1287A>G ENSP00000376773.2:n.565+1287A>G
ENST00000552831.1:n.643+1287A>G
ENST00000556029.5:c.565+1287A>G ENSP00000450627.1:n.565+1287A>G
ENST00000556678.1:c.286+1287A>G ENSP00000451552.1:n.286+1287A>G
XM_005269132.2:c.565+1287A>G XP_005269189.1:n.565+1287A>G
XM_005269132.4:c.565+1287A>G XP_005269189.1:n.565+1287A>G
XM_017019914.2:c.-39A>G XP_016875403.1:n.-39A>G