Canonical Allele Identifier: CA464295497

Gene: TOPORS SMIM27

Linked Data

• dbSNP Id: rs1191969323
• gnomAD v3: 9-32551186-C-A
• gnomAD v4: 9-32551186-C-A
• MyVariant Identifiers: chr9:g.32551184C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.32551186C>A , CM000671.2:g.32551186C>A	GRCh38
NC_000009.11:g.32551184C>A , CM000671.1:g.32551184C>A	GRCh37
NC_000009.10:g.32541184C>A	NCBI36
NG_017050.1:g.6439G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360538.7:c.4-218G>T (TOPORS) MANE Select	ENSP00000353735.2:n.4-218G>T
ENST00000453396.5:n.43C>A (SMIM27)
ENST00000680198.1:c.4-218G>T	ENSP00000505143.1:n.4-218G>T
ENST00000681750.1:c.-240+179G>T	ENSP00000506413.1:n.-240+179G>T
ENST00000360538.6:c.4-218G>T (TOPORS)	ENSP00000353735.2:n.4-218G>T
ENST00000379858.1:c.3+1248G>T (TOPORS)	ENSP00000369187.1:n.3+1248G>T
NM_001195622.1:c.3+1248G>T (TOPORS)	NP_001182551.1:n.3+1248G>T
NM_005802.4:c.4-218G>T (TOPORS)	NP_005793.2:n.4-218G>T
NR_033991.1:n.43C>A (SMIM27)
NM_001349118.1:c.-709C>A (SMIM27)	NP_001336047.1:n.-709C>A
XM_024447368.1:c.193C>A (SMIM27)	XP_024303136.1:p.His65Asn
NM_005802.5:c.4-218G>T (TOPORS) MANE Select	NP_005793.2:n.4-218G>T
NM_001195622.2:c.3+1248G>T (TOPORS)	NP_001182551.1:n.3+1248G>T