Canonical Allele Identifier: CA4477971

Gene: TNPO3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128975927A>G , CM000669.2:g.128975927A>G	GRCh38
NC_000007.13:g.128615981A>G , CM000669.1:g.128615981A>G	GRCh37
NC_000007.12:g.128403217A>G	NCBI36
NG_023428.1:g.84247T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_012470.4:c.2070T>C MANE Select	NP_036602.1:p.Asn690=
ENST00000265388.10:c.2070T>C MANE Select	ENSP00000265388.5:p.Asn690=
NM_001191028.2:c.1878T>C	NP_001177957.2:p.Asn626=
NM_001191028.3:c.1878T>C	NP_001177957.2:p.Asn626=
NM_001382216.1:c.2172T>C	NP_001369145.1:p.Asn724=
NM_001382217.1:c.2151T>C	NP_001369146.1:p.Asn717=
NM_001382218.1:c.2070T>C	NP_001369147.1:p.Asn690=
NM_001382219.1:c.1962T>C	NP_001369148.1:p.Asn654=
NM_001382220.1:c.1929T>C	NP_001369149.1:p.Asn643=
NM_001382221.1:c.1926T>C	NP_001369150.1:p.Asn642=
NM_001382222.1:c.1923T>C	NP_001369151.1:p.Asn641=
NM_001382223.1:c.1878T>C	NP_001369152.1:p.Asn626=
NM_012470.3:c.2070T>C	NP_036602.1:p.Asn690=
NR_034053.2:n.2634T>C
NR_034053.3:n.2572T>C
NR_167911.1:n.2659T>C
NR_167912.1:n.2517T>C
NR_167913.1:n.2319T>C
NR_167914.1:n.2479T>C
NR_167915.1:n.2572T>C
NR_167916.1:n.2209T>C
NR_167917.1:n.2242T>C
NR_167918.1:n.2697T>C
NR_167919.1:n.2536T>C
NR_167920.1:n.2495T>C
NR_167921.1:n.2697T>C
NR_167922.1:n.2533T>C
NR_167923.1:n.2334T>C
NR_167924.1:n.2411T>C
NR_167925.1:n.2334T>C
NR_167926.1:n.2345T>C
NR_167927.1:n.2638T>C
ENST00000265388.9:c.2070T>C	ENSP00000265388.5:p.Asn690=
ENST00000471166.1:c.2172T>C	ENSP00000418267.1:p.Asn724=
ENST00000471234.5:c.1878T>C	ENSP00000418646.1:p.Asn626=
ENST00000482320.5:c.1872T>C	ENSP00000420089.1:p.Asn624=
ENST00000627585.2:c.2172T>C	ENSP00000487231.1:p.Asn724=
XM_011515989.1:c.1872T>C	XP_011514291.1:p.Asn624=