Canonical Allele Identifier: CA373379111

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806155A>C (hg19) ; chr9:g.35806158A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806158A>C , CM000671.2:g.35806158A>C	GRCh38
NC_000009.11:g.35806155A>C , CM000671.1:g.35806155A>C	GRCh37
NC_000009.10:g.35796155A>C	NCBI36
NG_009249.1:g.18750A>C
NG_047141.1:g.11115T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.337A>C
ENST00000448821.6:c.2297A>C	ENSP00000402902.2:p.Glu766Ala
ENST00000685871.1:c.2225A>C	ENSP00000509964.1:p.Glu742Ala
ENST00000686159.1:n.2336A>C
ENST00000686486.1:n.1467A>C
ENST00000687302.1:n.2411A>C
ENST00000687357.1:c.2150A>C	ENSP00000509549.1:p.Glu717Ala
ENST00000687625.1:n.1452A>C
ENST00000687787.1:c.2456A>C	ENSP00000509440.1:p.Glu819Ala
ENST00000688201.1:n.2254A>C
ENST00000688226.1:n.2229A>C
ENST00000688869.1:n.2603A>C
ENST00000689788.1:c.2091A>C	ENSP00000508973.1:n.2091A>C
ENST00000689898.1:c.2154A>C	ENSP00000509651.1:n.2154A>C
ENST00000690070.1:c.2381A>C	ENSP00000509654.1:p.Glu794Ala
ENST00000690267.1:c.2086A>C	ENSP00000510432.1:n.2086A>C
ENST00000690552.1:n.2158A>C
ENST00000691138.1:n.2086A>C
ENST00000691969.1:c.1797A>C	ENSP00000510244.1:n.1797A>C
ENST00000692232.1:n.3612A>C
ENST00000692233.1:c.2161A>C	ENSP00000509698.1:n.2161A>C
ENST00000692380.1:n.1452A>C
ENST00000692447.1:n.3413A>C
ENST00000693094.1:c.2297A>C	ENSP00000510161.1:p.Glu766Ala
ENST00000342694.7:c.2297A>C MANE Select	ENSP00000341083.2:p.Glu766Ala
ENST00000342694.6:c.2297A>C	ENSP00000341083.2:p.Glu766Ala
ENST00000421267.5:c.337A>C
ENST00000447210.5:c.74A>C	ENSP00000393029.1:p.Glu25Ala
ENST00000464810.5:n.2297A>C
NM_003995.3:c.2297A>C	NP_003986.2:p.Glu766Ala
XM_005251478.3:c.2306A>C	XP_005251535.1:p.Glu769Ala
XM_005251479.3:c.1319A>C	XP_005251536.1:p.Glu440Ala
XM_006716778.2:c.2234A>C	XP_006716841.1:p.Glu745Ala
XM_011517889.1:c.1319A>C	XP_011516191.1:p.Glu440Ala
XM_011517890.1:c.1319A>C	XP_011516192.1:p.Glu440Ala
XM_011517891.1:c.1319A>C	XP_011516193.1:p.Glu440Ala
XM_011517892.1:c.1319A>C	XP_011516194.1:p.Glu440Ala
XM_011517893.1:c.1319A>C	XP_011516195.1:p.Glu440Ala
XM_011517894.1:c.1319A>C	XP_011516196.1:p.Glu440Ala
XM_011517895.1:c.902A>C	XP_011516197.1:p.Glu301Ala
XM_024447556.1:c.2465A>C	XP_024303324.1:p.Glu822Ala
XM_024447557.1:c.2456A>C	XP_024303325.1:p.Glu819Ala
XM_024447558.1:c.1478A>C	XP_024303326.1:p.Glu493Ala
XM_024447559.1:c.1061A>C	XP_024303327.1:p.Glu354Ala
XM_024447560.1:c.1052A>C	XP_024303328.1:p.Glu351Ala
XM_024447561.1:c.893A>C	XP_024303329.1:p.Glu298Ala
NM_003995.4:c.2297A>C MANE Select	NP_003986.2:p.Glu766Ala
NM_001378923.1:c.2306A>C	NP_001365852.1:p.Glu769Ala