Canonical Allele Identifier: CA373378706

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806060A>T (hg19) ; chr9:g.35806063A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806063A>T , CM000671.2:g.35806063A>T	GRCh38
NC_000009.11:g.35806060A>T , CM000671.1:g.35806060A>T	GRCh37
NC_000009.10:g.35796060A>T	NCBI36
NG_009249.1:g.18655A>T
NG_047141.1:g.11210T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.244-2A>T
ENST00000448821.6:c.2204-2A>T	ENSP00000402902.2:n.2204-2A>T
ENST00000685871.1:c.2132-2A>T	ENSP00000509964.1:n.2132-2A>T
ENST00000686159.1:n.2243-2A>T
ENST00000686486.1:n.1374-2A>T
ENST00000687302.1:n.2318-2A>T
ENST00000687357.1:c.2057-2A>T	ENSP00000509549.1:n.2057-2A>T
ENST00000687625.1:n.1359-2A>T
ENST00000687787.1:c.2363-2A>T	ENSP00000509440.1:n.2363-2A>T
ENST00000688201.1:n.2161-2A>T
ENST00000688226.1:n.2136-2A>T
ENST00000688869.1:n.2510-2A>T
ENST00000689788.1:c.1998-2A>T	ENSP00000508973.1:n.1998-2A>T
ENST00000689898.1:c.2061-2A>T	ENSP00000509651.1:n.2061-2A>T
ENST00000690070.1:c.2288-2A>T	ENSP00000509654.1:n.2288-2A>T
ENST00000690267.1:c.1993-2A>T	ENSP00000510432.1:n.1993-2A>T
ENST00000690552.1:n.2065-2A>T
ENST00000691138.1:n.1993-2A>T
ENST00000691969.1:c.1704-2A>T	ENSP00000510244.1:n.1704-2A>T
ENST00000692232.1:n.3519-2A>T
ENST00000692233.1:c.2068-2A>T	ENSP00000509698.1:n.2068-2A>T
ENST00000692380.1:n.1359-2A>T
ENST00000692447.1:n.3320-2A>T
ENST00000693094.1:c.2204-2A>T	ENSP00000510161.1:n.2204-2A>T
ENST00000342694.7:c.2204-2A>T MANE Select	ENSP00000341083.2:n.2204-2A>T
ENST00000342694.6:c.2204-2A>T	ENSP00000341083.2:n.2204-2A>T
ENST00000421267.5:c.244-2A>T
ENST00000464810.5:n.2204-2A>T
NM_003995.3:c.2204-2A>T	NP_003986.2:n.2204-2A>T
XM_005251478.3:c.2213-2A>T	XP_005251535.1:n.2213-2A>T
XM_005251479.3:c.1226-2A>T	XP_005251536.1:n.1226-2A>T
XM_006716778.2:c.2141-2A>T	XP_006716841.1:n.2141-2A>T
XM_011517889.1:c.1226-2A>T	XP_011516191.1:n.1226-2A>T
XM_011517890.1:c.1226-2A>T	XP_011516192.1:n.1226-2A>T
XM_011517891.1:c.1226-2A>T	XP_011516193.1:n.1226-2A>T
XM_011517892.1:c.1226-2A>T	XP_011516194.1:n.1226-2A>T
XM_011517893.1:c.1226-2A>T	XP_011516195.1:n.1226-2A>T
XM_011517894.1:c.1226-2A>T	XP_011516196.1:n.1226-2A>T
XM_011517895.1:c.809-2A>T	XP_011516197.1:n.809-2A>T
XM_024447556.1:c.2372-2A>T	XP_024303324.1:n.2372-2A>T
XM_024447557.1:c.2363-2A>T	XP_024303325.1:n.2363-2A>T
XM_024447558.1:c.1385-2A>T	XP_024303326.1:n.1385-2A>T
XM_024447559.1:c.968-2A>T	XP_024303327.1:n.968-2A>T
XM_024447560.1:c.959-2A>T	XP_024303328.1:n.959-2A>T
XM_024447561.1:c.800-2A>T	XP_024303329.1:n.800-2A>T
NM_003995.4:c.2204-2A>T MANE Select	NP_003986.2:n.2204-2A>T
NM_001378923.1:c.2213-2A>T	NP_001365852.1:n.2213-2A>T