Canonical Allele Identifier: CA1844698981

Gene: TOPORS SMIM27

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.32551128_32551129delinsCA , CM000671.2:g.32551128_32551129delinsCA	GRCh38
NC_000009.11:g.32551126_32551127delinsCA , CM000671.1:g.32551126_32551127delinsCA	GRCh37
NC_000009.10:g.32541126_32541127delinsCA	NCBI36
NG_017050.1:g.6496_6497delinsTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360538.7:c.4-161_4-160delinsTG (TOPORS) MANE Select	ENSP00000353735.2:n.4-161_4-160delinsTG
ENST00000680198.1:c.4-161_4-160delinsTG	ENSP00000505143.1:n.4-161_4-160delinsTG
ENST00000681750.1:c.-239-161_-239-160delinsTG	ENSP00000506413.1:n.-239-161_-239-160delinsTG
ENST00000360538.6:c.4-161_4-160delinsTG (TOPORS)	ENSP00000353735.2:n.4-161_4-160delinsTG
ENST00000379858.1:c.3+1305_3+1306delinsTG (TOPORS)	ENSP00000369187.1:n.3+1305_3+1306delinsTG
NM_001195622.1:c.3+1305_3+1306delinsTG (TOPORS)	NP_001182551.1:n.3+1305_3+1306delinsTG
NM_005802.4:c.4-161_4-160delinsTG (TOPORS)	NP_005793.2:n.4-161_4-160delinsTG
XM_024447368.1:c.135_136delinsCA (SMIM27)	XP_024303136.1:p.Pro45=
NM_005802.5:c.4-161_4-160delinsTG (TOPORS) MANE Select	NP_005793.2:n.4-161_4-160delinsTG
NM_001195622.2:c.3+1305_3+1306delinsTG (TOPORS)	NP_001182551.1:n.3+1305_3+1306delinsTG