Canonical Allele Identifier: CA464615556

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806096A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806099A>T , CM000671.2:g.35806099A>T	GRCh38
NC_000009.11:g.35806096A>T , CM000671.1:g.35806096A>T	GRCh37
NC_000009.10:g.35796096A>T	NCBI36
NG_009249.1:g.18691A>T
NG_047141.1:g.11174T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.278A>T
ENST00000448821.6:c.2238A>T	ENSP00000402902.2:p.Pro746=
ENST00000685871.1:c.2166A>T	ENSP00000509964.1:p.Pro722=
ENST00000686159.1:n.2277A>T
ENST00000686486.1:n.1408A>T
ENST00000687302.1:n.2352A>T
ENST00000687357.1:c.2091A>T	ENSP00000509549.1:p.Pro697=
ENST00000687625.1:n.1393A>T
ENST00000687787.1:c.2397A>T	ENSP00000509440.1:p.Pro799=
ENST00000688201.1:n.2195A>T
ENST00000688226.1:n.2170A>T
ENST00000688869.1:n.2544A>T
ENST00000689788.1:c.2032A>T	ENSP00000508973.1:n.2032A>T
ENST00000689898.1:c.2095A>T	ENSP00000509651.1:n.2095A>T
ENST00000690070.1:c.2322A>T	ENSP00000509654.1:p.Pro774=
ENST00000690267.1:c.2027A>T	ENSP00000510432.1:n.2027A>T
ENST00000690552.1:n.2099A>T
ENST00000691138.1:n.2027A>T
ENST00000691969.1:c.1738A>T	ENSP00000510244.1:n.1738A>T
ENST00000692232.1:n.3553A>T
ENST00000692233.1:c.2102A>T	ENSP00000509698.1:n.2102A>T
ENST00000692380.1:n.1393A>T
ENST00000692447.1:n.3354A>T
ENST00000693094.1:c.2238A>T	ENSP00000510161.1:p.Pro746=
ENST00000342694.7:c.2238A>T MANE Select	ENSP00000341083.2:p.Pro746=
ENST00000342694.6:c.2238A>T	ENSP00000341083.2:p.Pro746=
ENST00000421267.5:c.278A>T
ENST00000447210.5:c.15A>T	ENSP00000393029.1:p.Pro5=
ENST00000464810.5:n.2238A>T
NM_003995.3:c.2238A>T	NP_003986.2:p.Pro746=
XM_005251478.3:c.2247A>T	XP_005251535.1:p.Pro749=
XM_005251479.3:c.1260A>T	XP_005251536.1:p.Pro420=
XM_006716778.2:c.2175A>T	XP_006716841.1:p.Pro725=
XM_011517889.1:c.1260A>T	XP_011516191.1:p.Pro420=
XM_011517890.1:c.1260A>T	XP_011516192.1:p.Pro420=
XM_011517891.1:c.1260A>T	XP_011516193.1:p.Pro420=
XM_011517892.1:c.1260A>T	XP_011516194.1:p.Pro420=
XM_011517893.1:c.1260A>T	XP_011516195.1:p.Pro420=
XM_011517894.1:c.1260A>T	XP_011516196.1:p.Pro420=
XM_011517895.1:c.843A>T	XP_011516197.1:p.Pro281=
XM_024447556.1:c.2406A>T	XP_024303324.1:p.Pro802=
XM_024447557.1:c.2397A>T	XP_024303325.1:p.Pro799=
XM_024447558.1:c.1419A>T	XP_024303326.1:p.Pro473=
XM_024447559.1:c.1002A>T	XP_024303327.1:p.Pro334=
XM_024447560.1:c.993A>T	XP_024303328.1:p.Pro331=
XM_024447561.1:c.834A>T	XP_024303329.1:p.Pro278=
NM_003995.4:c.2238A>T MANE Select	NP_003986.2:p.Pro746=
NM_001378923.1:c.2247A>T	NP_001365852.1:p.Pro749=