Canonical Allele Identifier: CA464295511

Gene: TOPORS SMIM27

Linked Data

• MyVariant Identifiers: chr9:g.32551188T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.32551190T>G , CM000671.2:g.32551190T>G	GRCh38
NC_000009.11:g.32551188T>G , CM000671.1:g.32551188T>G	GRCh37
NC_000009.10:g.32541188T>G	NCBI36
NG_017050.1:g.6435A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360538.7:c.4-222A>C (TOPORS) MANE Select	ENSP00000353735.2:n.4-222A>C
ENST00000453396.5:n.47T>G (SMIM27)
ENST00000680198.1:c.4-222A>C	ENSP00000505143.1:n.4-222A>C
ENST00000681750.1:c.-240+175A>C	ENSP00000506413.1:n.-240+175A>C
ENST00000360538.6:c.4-222A>C (TOPORS)	ENSP00000353735.2:n.4-222A>C
ENST00000379858.1:c.3+1244A>C (TOPORS)	ENSP00000369187.1:n.3+1244A>C
NM_001195622.1:c.3+1244A>C (TOPORS)	NP_001182551.1:n.3+1244A>C
NM_005802.4:c.4-222A>C (TOPORS)	NP_005793.2:n.4-222A>C
NR_033991.1:n.47T>G (SMIM27)
NM_001349118.1:c.-705T>G (SMIM27)	NP_001336047.1:n.-705T>G
XM_024447368.1:c.197T>G (SMIM27)	XP_024303136.1:p.Leu66Arg
NM_005802.5:c.4-222A>C (TOPORS) MANE Select	NP_005793.2:n.4-222A>C
NM_001195622.2:c.3+1244A>C (TOPORS)	NP_001182551.1:n.3+1244A>C