Canonical Allele Identifier: CA373378888

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806115G>C (hg19) ; chr9:g.35806118G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806118G>C , CM000671.2:g.35806118G>C	GRCh38
NC_000009.11:g.35806115G>C , CM000671.1:g.35806115G>C	GRCh37
NC_000009.10:g.35796115G>C	NCBI36
NG_009249.1:g.18710G>C
NG_047141.1:g.11155C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.297G>C
ENST00000448821.6:c.2257G>C	ENSP00000402902.2:p.Asp753His
ENST00000685871.1:c.2185G>C	ENSP00000509964.1:p.Asp729His
ENST00000686159.1:n.2296G>C
ENST00000686486.1:n.1427G>C
ENST00000687302.1:n.2371G>C
ENST00000687357.1:c.2110G>C	ENSP00000509549.1:p.Asp704His
ENST00000687625.1:n.1412G>C
ENST00000687787.1:c.2416G>C	ENSP00000509440.1:p.Asp806His
ENST00000688201.1:n.2214G>C
ENST00000688226.1:n.2189G>C
ENST00000688869.1:n.2563G>C
ENST00000689788.1:c.2051G>C	ENSP00000508973.1:n.2051G>C
ENST00000689898.1:c.2114G>C	ENSP00000509651.1:n.2114G>C
ENST00000690070.1:c.2341G>C	ENSP00000509654.1:p.Asp781His
ENST00000690267.1:c.2046G>C	ENSP00000510432.1:n.2046G>C
ENST00000690552.1:n.2118G>C
ENST00000691138.1:n.2046G>C
ENST00000691969.1:c.1757G>C	ENSP00000510244.1:n.1757G>C
ENST00000692232.1:n.3572G>C
ENST00000692233.1:c.2121G>C	ENSP00000509698.1:n.2121G>C
ENST00000692380.1:n.1412G>C
ENST00000692447.1:n.3373G>C
ENST00000693094.1:c.2257G>C	ENSP00000510161.1:p.Asp753His
ENST00000342694.7:c.2257G>C MANE Select	ENSP00000341083.2:p.Asp753His
ENST00000342694.6:c.2257G>C	ENSP00000341083.2:p.Asp753His
ENST00000421267.5:c.297G>C
ENST00000447210.5:c.34G>C	ENSP00000393029.1:p.Asp12His
ENST00000464810.5:n.2257G>C
NM_003995.3:c.2257G>C	NP_003986.2:p.Asp753His
XM_005251478.3:c.2266G>C	XP_005251535.1:p.Asp756His
XM_005251479.3:c.1279G>C	XP_005251536.1:p.Asp427His
XM_006716778.2:c.2194G>C	XP_006716841.1:p.Asp732His
XM_011517889.1:c.1279G>C	XP_011516191.1:p.Asp427His
XM_011517890.1:c.1279G>C	XP_011516192.1:p.Asp427His
XM_011517891.1:c.1279G>C	XP_011516193.1:p.Asp427His
XM_011517892.1:c.1279G>C	XP_011516194.1:p.Asp427His
XM_011517893.1:c.1279G>C	XP_011516195.1:p.Asp427His
XM_011517894.1:c.1279G>C	XP_011516196.1:p.Asp427His
XM_011517895.1:c.862G>C	XP_011516197.1:p.Asp288His
XM_024447556.1:c.2425G>C	XP_024303324.1:p.Asp809His
XM_024447557.1:c.2416G>C	XP_024303325.1:p.Asp806His
XM_024447558.1:c.1438G>C	XP_024303326.1:p.Asp480His
XM_024447559.1:c.1021G>C	XP_024303327.1:p.Asp341His
XM_024447560.1:c.1012G>C	XP_024303328.1:p.Asp338His
XM_024447561.1:c.853G>C	XP_024303329.1:p.Asp285His
NM_003995.4:c.2257G>C MANE Select	NP_003986.2:p.Asp753His
NM_001378923.1:c.2266G>C	NP_001365852.1:p.Asp756His