Canonical Allele Identifier: CA373379381

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806207G>C (hg19) ; chr9:g.35806210G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806210G>C , CM000671.2:g.35806210G>C	GRCh38
NC_000009.11:g.35806207G>C , CM000671.1:g.35806207G>C	GRCh37
NC_000009.10:g.35796207G>C	NCBI36
NG_009249.1:g.18802G>C
NG_047141.1:g.11063C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.389G>C
ENST00000448821.6:c.2349G>C	ENSP00000402902.2:p.Lys783Asn
ENST00000685871.1:c.2277G>C	ENSP00000509964.1:p.Lys759Asn
ENST00000686159.1:n.2388G>C
ENST00000686486.1:n.1519G>C
ENST00000687302.1:n.2463G>C
ENST00000687357.1:c.2202G>C	ENSP00000509549.1:p.Lys734Asn
ENST00000687625.1:n.1504G>C
ENST00000687787.1:c.2508G>C	ENSP00000509440.1:p.Lys836Asn
ENST00000688201.1:n.2306G>C
ENST00000688226.1:n.2281G>C
ENST00000688869.1:n.2655G>C
ENST00000689788.1:c.2143G>C	ENSP00000508973.1:n.2143G>C
ENST00000689898.1:c.2206G>C	ENSP00000509651.1:n.2206G>C
ENST00000690070.1:c.2433G>C	ENSP00000509654.1:p.Lys811Asn
ENST00000690267.1:c.2138G>C	ENSP00000510432.1:n.2138G>C
ENST00000690552.1:n.2210G>C
ENST00000691138.1:n.2138G>C
ENST00000691969.1:c.1849G>C	ENSP00000510244.1:n.1849G>C
ENST00000692232.1:n.3664G>C
ENST00000692233.1:c.2213G>C	ENSP00000509698.1:n.2213G>C
ENST00000692380.1:n.1504G>C
ENST00000692447.1:n.3465G>C
ENST00000693094.1:c.2349G>C	ENSP00000510161.1:p.Lys783Asn
ENST00000342694.7:c.2349G>C MANE Select	ENSP00000341083.2:p.Lys783Asn
ENST00000342694.6:c.2349G>C	ENSP00000341083.2:p.Lys783Asn
ENST00000421267.5:c.389G>C
ENST00000447210.5:c.126G>C	ENSP00000393029.1:p.Lys42Asn
ENST00000464810.5:n.2349G>C
NM_003995.3:c.2349G>C	NP_003986.2:p.Lys783Asn
XM_005251478.3:c.2358G>C	XP_005251535.1:p.Lys786Asn
XM_005251479.3:c.1371G>C	XP_005251536.1:p.Lys457Asn
XM_006716778.2:c.2286G>C	XP_006716841.1:p.Lys762Asn
XM_011517889.1:c.1371G>C	XP_011516191.1:p.Lys457Asn
XM_011517890.1:c.1371G>C	XP_011516192.1:p.Lys457Asn
XM_011517891.1:c.1371G>C	XP_011516193.1:p.Lys457Asn
XM_011517892.1:c.1371G>C	XP_011516194.1:p.Lys457Asn
XM_011517893.1:c.1371G>C	XP_011516195.1:p.Lys457Asn
XM_011517894.1:c.1371G>C	XP_011516196.1:p.Lys457Asn
XM_011517895.1:c.954G>C	XP_011516197.1:p.Lys318Asn
XM_024447556.1:c.2517G>C	XP_024303324.1:p.Lys839Asn
XM_024447557.1:c.2508G>C	XP_024303325.1:p.Lys836Asn
XM_024447558.1:c.1530G>C	XP_024303326.1:p.Lys510Asn
XM_024447559.1:c.1113G>C	XP_024303327.1:p.Lys371Asn
XM_024447560.1:c.1104G>C	XP_024303328.1:p.Lys368Asn
XM_024447561.1:c.945G>C	XP_024303329.1:p.Lys315Asn
NM_003995.4:c.2349G>C MANE Select	NP_003986.2:p.Lys783Asn
NM_001378923.1:c.2358G>C	NP_001365852.1:p.Lys786Asn