Canonical Allele Identifier: CA3146181922

Gene: TNPO3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128970204A= , CM000669.2:g.128970204A=	GRCh38
NC_000007.13:g.128610258A= , CM000669.1:g.128610258A=	GRCh37
NC_000007.12:g.128397494A=	NCBI36
NG_023428.1:g.89970T=

Transcript Alleles

HGVS	Amino-acid Change
NM_012470.4:c.2542T= MANE Select	NP_036602.1:p.Tyr848=
ENST00000265388.10:c.2542T= MANE Select	ENSP00000265388.5:p.Tyr848=
NM_001191028.2:c.2350T=	NP_001177957.2:p.Tyr784=
NM_001191028.3:c.2350T=	NP_001177957.2:p.Tyr784=
NM_001382216.1:c.2644T=	NP_001369145.1:p.Tyr882=
NM_001382217.1:c.2623T=	NP_001369146.1:p.Tyr875=
NM_001382218.1:c.2542T=	NP_001369147.1:p.Tyr848=
NM_001382219.1:c.2434T=	NP_001369148.1:p.Tyr812=
NM_001382220.1:c.2401T=	NP_001369149.1:p.Tyr801=
NM_001382221.1:c.2398T=	NP_001369150.1:p.Tyr800=
NM_001382222.1:c.2395T=	NP_001369151.1:p.Tyr799=
NM_001382223.1:c.2350T=	NP_001369152.1:p.Tyr784=
NM_012470.3:c.2542T=	NP_036602.1:p.Tyr848=
NR_034053.2:n.3106T=
NR_034053.3:n.3044T=
NR_167911.1:n.3131T=
NR_167912.1:n.2989T=
NR_167913.1:n.2791T=
NR_167914.1:n.2951T=
NR_167915.1:n.3207T=
NR_167916.1:n.2681T=
NR_167917.1:n.2714T=
NR_167918.1:n.3169T=
NR_167919.1:n.3008T=
NR_167920.1:n.2967T=
NR_167921.1:n.3169T=
NR_167922.1:n.3005T=
NR_167923.1:n.2806T=
NR_167924.1:n.2883T=
NR_167925.1:n.2806T=
NR_167926.1:n.2817T=
NR_167927.1:n.3110T=
ENST00000265388.9:c.2542T=	ENSP00000265388.5:p.Tyr848=
ENST00000471166.1:c.2644T=	ENSP00000418267.1:p.Tyr882=
ENST00000471234.5:c.2350T=	ENSP00000418646.1:p.Tyr784=
ENST00000482320.5:c.2344T=	ENSP00000420089.1:p.Tyr782=
ENST00000627585.2:c.2644T=	ENSP00000487231.1:p.Tyr882=
XM_011515989.1:c.2344T=	XP_011514291.1:p.Tyr782=