Canonical Allele Identifier: CA373379733

Gene: NPR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806433T>A , CM000671.2:g.35806433T>A	GRCh38
NC_000009.11:g.35806430T>A , CM000671.1:g.35806430T>A	GRCh37
NC_000009.10:g.35796430T>A	NCBI36
NG_009249.1:g.19025T>A
NG_047141.1:g.10840A>T

Transcript Alleles

HGVS	Amino-acid Change
NM_003995.4:c.2414T>A MANE Select	NP_003986.2:p.Met805Lys
ENST00000342694.7:c.2414T>A MANE Select	ENSP00000341083.2:p.Met805Lys
NM_001378923.1:c.2423T>A	NP_001365852.1:p.Met808Lys
NM_003995.3:c.2414T>A	NP_003986.2:p.Met805Lys
ENST00000342694.6:c.2414T>A	ENSP00000341083.2:p.Met805Lys
ENST00000421267.5:c.454T>A
ENST00000421267.6:c.454T>A
ENST00000447210.5:c.191T>A	ENSP00000393029.1:p.Met64Lys
ENST00000448821.6:c.2414T>A	ENSP00000402902.2:p.Met805Lys
ENST00000464810.5:n.2414T>A
ENST00000685871.1:c.2342T>A	ENSP00000509964.1:p.Met781Lys
ENST00000686159.1:n.2453T>A
ENST00000686486.1:n.1584T>A
ENST00000687302.1:n.2528T>A
ENST00000687357.1:c.2267T>A	ENSP00000509549.1:p.Met756Lys
ENST00000687625.1:n.1569T>A
ENST00000687787.1:c.2573T>A	ENSP00000509440.1:p.Met858Lys
ENST00000688201.1:n.2371T>A
ENST00000688226.1:n.2346T>A
ENST00000688869.1:n.2720T>A
ENST00000689788.1:c.2208T>A	ENSP00000508973.1:n.2208T>A
ENST00000689898.1:c.2271T>A	ENSP00000509651.1:n.2271T>A
ENST00000690070.1:c.2498T>A	ENSP00000509654.1:p.Met833Lys
ENST00000690267.1:c.2203T>A	ENSP00000510432.1:n.2203T>A
ENST00000690552.1:n.2275T>A
ENST00000691138.1:n.2203T>A
ENST00000691969.1:c.1914T>A	ENSP00000510244.1:n.1914T>A
ENST00000692232.1:n.3729T>A
ENST00000692233.1:c.2278T>A	ENSP00000509698.1:n.2278T>A
ENST00000692380.1:n.1569T>A
ENST00000692447.1:n.3530T>A
ENST00000693094.1:c.2414T>A	ENSP00000510161.1:p.Met805Lys
XM_005251478.3:c.2423T>A	XP_005251535.1:p.Met808Lys
XM_005251479.3:c.1436T>A	XP_005251536.1:p.Met479Lys
XM_006716778.2:c.2351T>A	XP_006716841.1:p.Met784Lys
XM_011517889.1:c.1436T>A	XP_011516191.1:p.Met479Lys
XM_011517890.1:c.1436T>A	XP_011516192.1:p.Met479Lys
XM_011517891.1:c.1436T>A	XP_011516193.1:p.Met479Lys
XM_011517892.1:c.1436T>A	XP_011516194.1:p.Met479Lys
XM_011517893.1:c.1436T>A	XP_011516195.1:p.Met479Lys
XM_011517894.1:c.1436T>A	XP_011516196.1:p.Met479Lys
XM_011517895.1:c.1019T>A	XP_011516197.1:p.Met340Lys
XM_024447556.1:c.2582T>A	XP_024303324.1:p.Met861Lys
XM_024447557.1:c.2573T>A	XP_024303325.1:p.Met858Lys
XM_024447558.1:c.1595T>A	XP_024303326.1:p.Met532Lys
XM_024447559.1:c.1178T>A	XP_024303327.1:p.Met393Lys
XM_024447560.1:c.1169T>A	XP_024303328.1:p.Met390Lys
XM_024447561.1:c.1010T>A	XP_024303329.1:p.Met337Lys