Canonical Allele Identifier: CA587565253

Gene: TOPORS SMIM27

Linked Data

• dbSNP Id: rs1301206941
• gnomAD v2: 9-32551001-C-T
• gnomAD v4: 9-32551003-C-T
• MyVariant Identifiers: chr9:g.32551001C>T (hg19) ; chr9:g.32551003C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.32551003C>T , CM000671.2:g.32551003C>T	GRCh38
NC_000009.11:g.32551001C>T , CM000671.1:g.32551001C>T	GRCh37
NC_000009.10:g.32541001C>T	NCBI36
NG_017050.1:g.6622G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360538.7:c.4-35G>A (TOPORS) MANE Select	ENSP00000353735.2:n.4-35G>A
ENST00000680198.1:c.4-35G>A	ENSP00000505143.1:n.4-35G>A
ENST00000681750.1:c.-239-35G>A	ENSP00000506413.1:n.-239-35G>A
ENST00000360538.6:c.4-35G>A (TOPORS)	ENSP00000353735.2:n.4-35G>A
ENST00000379858.1:c.3+1431G>A (TOPORS)	ENSP00000369187.1:n.3+1431G>A
NM_001195622.1:c.3+1431G>A (TOPORS)	NP_001182551.1:n.3+1431G>A
NM_005802.4:c.4-35G>A (TOPORS)	NP_005793.2:n.4-35G>A
XM_024447368.1:c.10C>T (SMIM27)	XP_024303136.1:p.Arg4Trp
NM_005802.5:c.4-35G>A (TOPORS) MANE Select	NP_005793.2:n.4-35G>A
NM_001195622.2:c.3+1431G>A (TOPORS)	NP_001182551.1:n.3+1431G>A