Canonical Allele Identifier: CA386154557

Gene: TMPO

Linked Data

• dbSNP Id: rs1300565394
• gnomAD v3: 12-98534332-A-G
• gnomAD v4: 12-98534332-A-G
• MyVariant Identifiers: chr12:g.98928110A>G (hg19) ; chr12:g.98534332A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.98534332A>G , CM000674.2:g.98534332A>G	GRCh38
NC_000012.11:g.98928110A>G , CM000674.1:g.98928110A>G	GRCh37
NC_000012.10:g.97452241A>G	NCBI36
NG_021393.1:g.23760A>G , LRG_443:g.23760A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000556029.6:c.565+2494A>G MANE Select	ENSP00000450627.1:n.565+2494A>G
ENST00000261210.9:c.565+2494A>G	ENSP00000261210.5:n.565+2494A>G
ENST00000266732.8:c.2075A>G	ENSP00000266732.4:p.Asn692Ser
ENST00000343315.9:c.565+2494A>G	ENSP00000340251.5:n.565+2494A>G
ENST00000393053.6:c.565+2494A>G	ENSP00000376773.2:n.565+2494A>G
ENST00000552831.1:n.643+2494A>G
ENST00000556029.5:c.565+2494A>G	ENSP00000450627.1:n.565+2494A>G
ENST00000556678.1:c.286+2494A>G	ENSP00000451552.1:n.286+2494A>G
NM_001032283.2:c.565+2494A>G , LRG_443t1:c.565+2494A>G	NP_001027454.1:n.565+2494A>G
NM_001032284.2:c.565+2494A>G	NP_001027455.1:n.565+2494A>G
NM_001307975.1:c.565+2494A>G	NP_001294904.1:n.565+2494A>G
NM_003276.2:c.2075A>G , LRG_443t2:c.2075A>G	NP_003267.1:p.Asn692Ser
XM_005269132.2:c.565+2494A>G	XP_005269189.1:n.565+2494A>G
XM_005269132.4:c.565+2494A>G	XP_005269189.1:n.565+2494A>G
XM_017019914.2:c.1169A>G	XP_016875403.1:p.Asn390Ser
NM_001032283.3:c.565+2494A>G MANE Select	NP_001027454.1:n.565+2494A>G
NM_001032284.3:c.565+2494A>G	NP_001027455.1:n.565+2494A>G
NM_001307975.2:c.565+2494A>G	NP_001294904.1:n.565+2494A>G