Canonical Allele Identifier: CA464295413

Gene: TOPORS SMIM27

Linked Data

• MyVariant Identifiers: chr9:g.32551153A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.32551155A>C , CM000671.2:g.32551155A>C	GRCh38
NC_000009.11:g.32551153A>C , CM000671.1:g.32551153A>C	GRCh37
NC_000009.10:g.32541153A>C	NCBI36
NG_017050.1:g.6470T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360538.7:c.4-187T>G (TOPORS) MANE Select	ENSP00000353735.2:n.4-187T>G
ENST00000453396.5:n.12A>C (SMIM27)
ENST00000680198.1:c.4-187T>G	ENSP00000505143.1:n.4-187T>G
ENST00000681750.1:c.-239-187T>G	ENSP00000506413.1:n.-239-187T>G
ENST00000360538.6:c.4-187T>G (TOPORS)	ENSP00000353735.2:n.4-187T>G
ENST00000379858.1:c.3+1279T>G (TOPORS)	ENSP00000369187.1:n.3+1279T>G
NM_001195622.1:c.3+1279T>G (TOPORS)	NP_001182551.1:n.3+1279T>G
NM_005802.4:c.4-187T>G (TOPORS)	NP_005793.2:n.4-187T>G
NR_033991.1:n.12A>C (SMIM27)
NM_001349118.1:c.-740A>C (SMIM27)	NP_001336047.1:n.-740A>C
XM_024447368.1:c.162A>C (SMIM27)	XP_024303136.1:p.Pro54=
NM_005802.5:c.4-187T>G (TOPORS) MANE Select	NP_005793.2:n.4-187T>G
NM_001195622.2:c.3+1279T>G (TOPORS)	NP_001182551.1:n.3+1279T>G