Canonical Allele Identifier: CA481444734

Gene: TMPO

Linked Data

• gnomAD v4: 12-98534330-A-C
• MyVariant Identifiers: chr12:g.98928108A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.98534330A>C , CM000674.2:g.98534330A>C	GRCh38
NC_000012.11:g.98928108A>C , CM000674.1:g.98928108A>C	GRCh37
NC_000012.10:g.97452239A>C	NCBI36
NG_021393.1:g.23758A>C , LRG_443:g.23758A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000556029.6:c.565+2492A>C MANE Select	ENSP00000450627.1:n.565+2492A>C
ENST00000261210.9:c.565+2492A>C	ENSP00000261210.5:n.565+2492A>C
ENST00000266732.8:c.2073A>C	ENSP00000266732.4:p.Gly691=
ENST00000343315.9:c.565+2492A>C	ENSP00000340251.5:n.565+2492A>C
ENST00000393053.6:c.565+2492A>C	ENSP00000376773.2:n.565+2492A>C
ENST00000552831.1:n.643+2492A>C
ENST00000556029.5:c.565+2492A>C	ENSP00000450627.1:n.565+2492A>C
ENST00000556678.1:c.286+2492A>C	ENSP00000451552.1:n.286+2492A>C
NM_001032283.2:c.565+2492A>C , LRG_443t1:c.565+2492A>C	NP_001027454.1:n.565+2492A>C
NM_001032284.2:c.565+2492A>C	NP_001027455.1:n.565+2492A>C
NM_001307975.1:c.565+2492A>C	NP_001294904.1:n.565+2492A>C
NM_003276.2:c.2073A>C , LRG_443t2:c.2073A>C	NP_003267.1:p.Gly691=
XM_005269132.2:c.565+2492A>C	XP_005269189.1:n.565+2492A>C
XM_005269132.4:c.565+2492A>C	XP_005269189.1:n.565+2492A>C
XM_017019914.2:c.1167A>C	XP_016875403.1:p.Gly389=
NM_001032283.3:c.565+2492A>C MANE Select	NP_001027454.1:n.565+2492A>C
NM_001032284.3:c.565+2492A>C	NP_001027455.1:n.565+2492A>C
NM_001307975.2:c.565+2492A>C	NP_001294904.1:n.565+2492A>C