Canonical Allele Identifier: CA2783454051

Gene: TOPORS SMIM27

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.32551123_32551124insACA , CM000671.2:g.32551123_32551124insACA	GRCh38
NC_000009.11:g.32551121_32551122insACA , CM000671.1:g.32551121_32551122insACA	GRCh37
NC_000009.10:g.32541121_32541122insACA	NCBI36
NG_017050.1:g.6501_6502insTGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360538.7:c.4-156_4-155insTGT (TOPORS) MANE Select	ENSP00000353735.2:n.4-156_4-155insTGT
ENST00000680198.1:c.4-156_4-155insTGT	ENSP00000505143.1:n.4-156_4-155insTGT
ENST00000681750.1:c.-239-156_-239-155insTGT	ENSP00000506413.1:n.-239-156_-239-155insTGT
ENST00000360538.6:c.4-156_4-155insTGT (TOPORS)	ENSP00000353735.2:n.4-156_4-155insTGT
ENST00000379858.1:c.3+1310_3+1311insTGT (TOPORS)	ENSP00000369187.1:n.3+1310_3+1311insTGT
NM_001195622.1:c.3+1310_3+1311insTGT (TOPORS)	NP_001182551.1:n.3+1310_3+1311insTGT
NM_005802.4:c.4-156_4-155insTGT (TOPORS)	NP_005793.2:n.4-156_4-155insTGT
XM_024447368.1:c.130_131insACA (SMIM27)	XP_024303136.1:p.His43_Arg44insHis
NM_005802.5:c.4-156_4-155insTGT (TOPORS) MANE Select	NP_005793.2:n.4-156_4-155insTGT
NM_001195622.2:c.3+1310_3+1311insTGT (TOPORS)	NP_001182551.1:n.3+1310_3+1311insTGT