Canonical Allele Identifier: CA481589996

Gene: TMPO TMPO-AS1

Linked Data

• MyVariant Identifiers: chr12:g.98909963G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.98516185G>C , CM000674.2:g.98516185G>C	GRCh38
NC_000012.11:g.98909963G>C , CM000674.1:g.98909963G>C	GRCh37
NC_000012.10:g.97434094G>C	NCBI36
NG_021393.1:g.5613G>C , LRG_443:g.5613G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000556029.6:c.279+39G>C (TMPO) MANE Select	ENSP00000450627.1:n.279+39G>C
ENST00000261210.9:c.279+39G>C (TMPO)	ENSP00000261210.5:n.279+39G>C
ENST00000266732.8:c.279+39G>C (TMPO)	ENSP00000266732.4:n.279+39G>C
ENST00000343315.9:c.279+39G>C (TMPO)	ENSP00000340251.5:n.279+39G>C
ENST00000393053.6:c.279+39G>C (TMPO)	ENSP00000376773.2:n.279+39G>C
ENST00000546828.6:n.337+39G>C (TMPO)
ENST00000548911.1:n.412+39G>C (TMPO)
ENST00000556029.5:c.279+39G>C (TMPO)	ENSP00000450627.1:n.279+39G>C
NM_001032283.2:c.279+39G>C , LRG_443t1:c.279+39G>C (TMPO)	NP_001027454.1:n.279+39G>C
NM_001032284.2:c.279+39G>C (TMPO)	NP_001027455.1:n.279+39G>C
NM_001307975.1:c.279+39G>C (TMPO)	NP_001294904.1:n.279+39G>C
NM_003276.2:c.279+39G>C , LRG_443t2:c.279+39G>C (TMPO)	NP_003267.1:n.279+39G>C
NR_027157.1:n.42C>G (TMPO-AS1)
XM_005269132.2:c.279+39G>C (TMPO)	XP_005269189.1:n.279+39G>C
XM_005269132.4:c.279+39G>C (TMPO)	XP_005269189.1:n.279+39G>C
NM_001032283.3:c.279+39G>C (TMPO) MANE Select	NP_001027454.1:n.279+39G>C
NM_001032284.3:c.279+39G>C (TMPO)	NP_001027455.1:n.279+39G>C
NM_001307975.2:c.279+39G>C (TMPO)	NP_001294904.1:n.279+39G>C