Canonical Allele Identifier: CA1742576269

Gene: TNPO3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128954242G= , CM000669.2:g.128954242G=	GRCh38
NC_000007.13:g.128594296G= , CM000669.1:g.128594296G=	GRCh37
NC_000007.12:g.128381532G=	NCBI36
NG_023428.1:g.105932C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000265388.10:c.*1175C= MANE Select	ENSP00000265388.5:n.*1175C=
ENST00000265388.9:c.*1175C=	ENSP00000265388.5:n.*1175C=
ENST00000627585.2:c.*1175C=	ENSP00000487231.1:n.*1175C=
NM_001191028.2:c.*1175C=	NP_001177957.2:n.*1175C=
NM_012470.3:c.*1175C=	NP_036602.1:n.*1175C=
NR_034053.2:n.4511C=
XM_011515989.1:c.*1175C=	XP_011514291.1:n.*1175C=
NM_001191028.3:c.*1175C=	NP_001177957.2:n.*1175C=
NM_001382216.1:c.*1175C=	NP_001369145.1:n.*1175C=
NM_001382217.1:c.*1175C=	NP_001369146.1:n.*1175C=
NM_001382218.1:c.*1125C=	NP_001369147.1:n.*1125C=
NM_001382219.1:c.*1175C=	NP_001369148.1:n.*1175C=
NM_001382220.1:c.*1175C=	NP_001369149.1:n.*1175C=
NM_001382221.1:c.*1175C=	NP_001369150.1:n.*1175C=
NM_001382222.1:c.*1175C=	NP_001369151.1:n.*1175C=
NM_001382223.1:c.*1125C=	NP_001369152.1:n.*1125C=
NM_012470.4:c.*1175C= MANE Select	NP_036602.1:n.*1175C=
NR_034053.3:n.4449C=
NR_167911.1:n.4536C=
NR_167912.1:n.4394C=
NR_167913.1:n.4196C=
NR_167914.1:n.4356C=
NR_167915.1:n.4612C=
NR_167916.1:n.4086C=
NR_167917.1:n.4119C=
NR_167918.1:n.4574C=
NR_167919.1:n.4413C=
NR_167920.1:n.4372C=
NR_167921.1:n.4574C=
NR_167922.1:n.4410C=
NR_167923.1:n.4211C=
NR_167924.1:n.4439C=
NR_167925.1:n.4211C=
NR_167926.1:n.4222C=
NR_167927.1:n.4515C=