Canonical Allele Identifier: CA464615648

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806141A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806144A>C , CM000671.2:g.35806144A>C	GRCh38
NC_000009.11:g.35806141A>C , CM000671.1:g.35806141A>C	GRCh37
NC_000009.10:g.35796141A>C	NCBI36
NG_009249.1:g.18736A>C
NG_047141.1:g.11129T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.323A>C
ENST00000448821.6:c.2283A>C	ENSP00000402902.2:p.Leu761=
ENST00000685871.1:c.2211A>C	ENSP00000509964.1:p.Leu737=
ENST00000686159.1:n.2322A>C
ENST00000686486.1:n.1453A>C
ENST00000687302.1:n.2397A>C
ENST00000687357.1:c.2136A>C	ENSP00000509549.1:p.Leu712=
ENST00000687625.1:n.1438A>C
ENST00000687787.1:c.2442A>C	ENSP00000509440.1:p.Leu814=
ENST00000688201.1:n.2240A>C
ENST00000688226.1:n.2215A>C
ENST00000688869.1:n.2589A>C
ENST00000689788.1:c.2077A>C	ENSP00000508973.1:n.2077A>C
ENST00000689898.1:c.2140A>C	ENSP00000509651.1:n.2140A>C
ENST00000690070.1:c.2367A>C	ENSP00000509654.1:p.Leu789=
ENST00000690267.1:c.2072A>C	ENSP00000510432.1:n.2072A>C
ENST00000690552.1:n.2144A>C
ENST00000691138.1:n.2072A>C
ENST00000691969.1:c.1783A>C	ENSP00000510244.1:n.1783A>C
ENST00000692232.1:n.3598A>C
ENST00000692233.1:c.2147A>C	ENSP00000509698.1:n.2147A>C
ENST00000692380.1:n.1438A>C
ENST00000692447.1:n.3399A>C
ENST00000693094.1:c.2283A>C	ENSP00000510161.1:p.Leu761=
ENST00000342694.7:c.2283A>C MANE Select	ENSP00000341083.2:p.Leu761=
ENST00000342694.6:c.2283A>C	ENSP00000341083.2:p.Leu761=
ENST00000421267.5:c.323A>C
ENST00000447210.5:c.60A>C	ENSP00000393029.1:p.Leu20=
ENST00000464810.5:n.2283A>C
NM_003995.3:c.2283A>C	NP_003986.2:p.Leu761=
XM_005251478.3:c.2292A>C	XP_005251535.1:p.Leu764=
XM_005251479.3:c.1305A>C	XP_005251536.1:p.Leu435=
XM_006716778.2:c.2220A>C	XP_006716841.1:p.Leu740=
XM_011517889.1:c.1305A>C	XP_011516191.1:p.Leu435=
XM_011517890.1:c.1305A>C	XP_011516192.1:p.Leu435=
XM_011517891.1:c.1305A>C	XP_011516193.1:p.Leu435=
XM_011517892.1:c.1305A>C	XP_011516194.1:p.Leu435=
XM_011517893.1:c.1305A>C	XP_011516195.1:p.Leu435=
XM_011517894.1:c.1305A>C	XP_011516196.1:p.Leu435=
XM_011517895.1:c.888A>C	XP_011516197.1:p.Leu296=
XM_024447556.1:c.2451A>C	XP_024303324.1:p.Leu817=
XM_024447557.1:c.2442A>C	XP_024303325.1:p.Leu814=
XM_024447558.1:c.1464A>C	XP_024303326.1:p.Leu488=
XM_024447559.1:c.1047A>C	XP_024303327.1:p.Leu349=
XM_024447560.1:c.1038A>C	XP_024303328.1:p.Leu346=
XM_024447561.1:c.879A>C	XP_024303329.1:p.Leu293=
NM_003995.4:c.2283A>C MANE Select	NP_003986.2:p.Leu761=
NM_001378923.1:c.2292A>C	NP_001365852.1:p.Leu764=