Canonical Allele Identifier: CA457580896

Gene: TNPO3

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.128982283G>A , CM000669.2:g.128982283G>A	GRCh38
NC_000007.13:g.128622337G>A , CM000669.1:g.128622337G>A	GRCh37
NC_000007.12:g.128409573G>A	NCBI36
NG_023428.1:g.77891C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_012470.4:c.1824C>T MANE Select	NP_036602.1:p.Pro608=
ENST00000265388.10:c.1824C>T MANE Select	ENSP00000265388.5:p.Pro608=
NM_001191028.2:c.1632C>T	NP_001177957.2:p.Pro544=
NM_001191028.3:c.1632C>T	NP_001177957.2:p.Pro544=
NM_001382216.1:c.1926C>T	NP_001369145.1:p.Pro642=
NM_001382217.1:c.1905C>T	NP_001369146.1:p.Pro635=
NM_001382218.1:c.1824C>T	NP_001369147.1:p.Pro608=
NM_001382219.1:c.1716C>T	NP_001369148.1:p.Pro572=
NM_001382220.1:c.1824C>T	NP_001369149.1:p.Pro608=
NM_001382221.1:c.1680C>T	NP_001369150.1:p.Pro560=
NM_001382222.1:c.1677C>T	NP_001369151.1:p.Pro559=
NM_001382223.1:c.1632C>T	NP_001369152.1:p.Pro544=
NM_012470.3:c.1824C>T	NP_036602.1:p.Pro608=
NR_034053.2:n.2388C>T
NR_034053.3:n.2326C>T
NR_167911.1:n.2413C>T
NR_167912.1:n.2165C>T
NR_167913.1:n.2073C>T
NR_167914.1:n.2233C>T
NR_167915.1:n.2326C>T
NR_167916.1:n.2165C>T
NR_167917.1:n.2031+1885C>T
NR_167918.1:n.2451C>T
NR_167919.1:n.2290C>T
NR_167920.1:n.2451C>T
NR_167921.1:n.2451C>T
NR_167922.1:n.2287C>T
NR_167923.1:n.2290C>T
NR_167924.1:n.2165C>T
NR_167925.1:n.2123+1885C>T
NR_167926.1:n.2301C>T
NR_167927.1:n.2392C>T
ENST00000265388.9:c.1824C>T	ENSP00000265388.5:p.Pro608=
ENST00000471166.1:c.1926C>T	ENSP00000418267.1:p.Pro642=
ENST00000471234.5:c.1632C>T	ENSP00000418646.1:p.Pro544=
ENST00000482320.5:c.1626C>T	ENSP00000420089.1:p.Pro542=
ENST00000627585.2:c.1926C>T	ENSP00000487231.1:p.Pro642=
XM_011515989.1:c.1626C>T	XP_011514291.1:p.Pro542=