Canonical Allele Identifier: CA386154569

Gene: TMPO

Linked Data

• MyVariant Identifiers: chr12:g.98928115C>G (hg19) ; chr12:g.98534337C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.98534337C>G , CM000674.2:g.98534337C>G	GRCh38
NC_000012.11:g.98928115C>G , CM000674.1:g.98928115C>G	GRCh37
NC_000012.10:g.97452246C>G	NCBI36
NG_021393.1:g.23765C>G , LRG_443:g.23765C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556029.6:c.565+2499C>G MANE Select	ENSP00000450627.1:n.565+2499C>G
ENST00000261210.9:c.565+2499C>G	ENSP00000261210.5:n.565+2499C>G
ENST00000266732.8:c.2080C>G	ENSP00000266732.4:p.His694Asp
ENST00000343315.9:c.565+2499C>G	ENSP00000340251.5:n.565+2499C>G
ENST00000393053.6:c.565+2499C>G	ENSP00000376773.2:n.565+2499C>G
ENST00000552831.1:n.643+2499C>G
ENST00000556029.5:c.565+2499C>G	ENSP00000450627.1:n.565+2499C>G
ENST00000556678.1:c.286+2499C>G	ENSP00000451552.1:n.286+2499C>G
NM_001032283.2:c.565+2499C>G , LRG_443t1:c.565+2499C>G	NP_001027454.1:n.565+2499C>G
NM_001032284.2:c.565+2499C>G	NP_001027455.1:n.565+2499C>G
NM_001307975.1:c.565+2499C>G	NP_001294904.1:n.565+2499C>G
NM_003276.2:c.2080C>G , LRG_443t2:c.2080C>G	NP_003267.1:p.His694Asp
XM_005269132.2:c.565+2499C>G	XP_005269189.1:n.565+2499C>G
XM_005269132.4:c.565+2499C>G	XP_005269189.1:n.565+2499C>G
XM_017019914.2:c.1174C>G	XP_016875403.1:p.His392Asp
NM_001032283.3:c.565+2499C>G MANE Select	NP_001027454.1:n.565+2499C>G
NM_001032284.3:c.565+2499C>G	NP_001027455.1:n.565+2499C>G
NM_001307975.2:c.565+2499C>G	NP_001294904.1:n.565+2499C>G