Canonical Allele Identifier: CA1846131215

Gene: NPR2

Linked Data

• dbSNP Id: rs1828102461

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35800319_35800320insTCAGAG , CM000671.2:g.35800319_35800320insTCAGAG	GRCh38
NC_000009.11:g.35800316_35800317insTCAGAG , CM000671.1:g.35800316_35800317insTCAGAG	GRCh37
NC_000009.10:g.35790316_35790317insTCAGAG	NCBI36
NG_009249.1:g.12911_12912insTCAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448821.6:c.1124-70_1124-69insTCAGAG	ENSP00000402902.2:n.1124-70_1124-69insTCAGAG
ENST00000685871.1:c.1124-70_1124-69insTCAGAG	ENSP00000509964.1:n.1124-70_1124-69insTCAGAG
ENST00000686159.1:n.1163-70_1163-69insTCAGAG
ENST00000687302.1:n.985-70_985-69insTCAGAG
ENST00000687357.1:c.1124-70_1124-69insTCAGAG	ENSP00000509549.1:n.1124-70_1124-69insTCAGAG
ENST00000687625.1:n.279-70_279-69insTCAGAG
ENST00000687787.1:c.1124-70_1124-69insTCAGAG	ENSP00000509440.1:n.1124-70_1124-69insTCAGAG
ENST00000688201.1:n.1156-70_1156-69insTCAGAG
ENST00000688226.1:n.1056-70_1056-69insTCAGAG
ENST00000688869.1:n.1205-70_1205-69insTCAGAG
ENST00000689788.1:c.918-70_918-69insTCAGAG	ENSP00000508973.1:n.918-70_918-69insTCAGAG
ENST00000689898.1:c.1124-70_1124-69insTCAGAG	ENSP00000509651.1:n.1124-70_1124-69insTCAGAG
ENST00000690070.1:c.1124-70_1124-69insTCAGAG	ENSP00000509654.1:n.1124-70_1124-69insTCAGAG
ENST00000690267.1:c.988-70_988-69insTCAGAG	ENSP00000510432.1:n.988-70_988-69insTCAGAG
ENST00000690552.1:n.985-70_985-69insTCAGAG
ENST00000691138.1:n.985-70_985-69insTCAGAG
ENST00000691969.1:c.699-70_699-69insTCAGAG	ENSP00000510244.1:n.699-70_699-69insTCAGAG
ENST00000692232.1:n.1985_1986insTCAGAG
ENST00000692233.1:c.988-70_988-69insTCAGAG	ENSP00000509698.1:n.988-70_988-69insTCAGAG
ENST00000692380.1:n.279-70_279-69insTCAGAG
ENST00000692447.1:n.2236-70_2236-69insTCAGAG
ENST00000693094.1:c.1124-70_1124-69insTCAGAG	ENSP00000510161.1:n.1124-70_1124-69insTCAGAG
ENST00000342694.7:c.1124-70_1124-69insTCAGAG MANE Select	ENSP00000341083.2:n.1124-70_1124-69insTCAGAG
ENST00000342694.6:c.1124-70_1124-69insTCAGAG	ENSP00000341083.2:n.1124-70_1124-69insTCAGAG
ENST00000464810.5:n.1124-70_1124-69insTCAGAG
NM_003995.3:c.1124-70_1124-69insTCAGAG	NP_003986.2:n.1124-70_1124-69insTCAGAG
XM_005251478.3:c.1124-70_1124-69insTCAGAG	XP_005251535.1:n.1124-70_1124-69insTCAGAG
XM_005251479.3:c.137-70_137-69insTCAGAG	XP_005251536.1:n.137-70_137-69insTCAGAG
XM_006716778.2:c.1124-70_1124-69insTCAGAG	XP_006716841.1:n.1124-70_1124-69insTCAGAG
XM_011517889.1:c.137-70_137-69insTCAGAG	XP_011516191.1:n.137-70_137-69insTCAGAG
XM_011517890.1:c.137-70_137-69insTCAGAG	XP_011516192.1:n.137-70_137-69insTCAGAG
XM_011517891.1:c.137-70_137-69insTCAGAG	XP_011516193.1:n.137-70_137-69insTCAGAG
XM_011517892.1:c.137-70_137-69insTCAGAG	XP_011516194.1:n.137-70_137-69insTCAGAG
XM_011517893.1:c.137-70_137-69insTCAGAG	XP_011516195.1:n.137-70_137-69insTCAGAG
XM_011517894.1:c.137-70_137-69insTCAGAG	XP_011516196.1:n.137-70_137-69insTCAGAG
XM_024447556.1:c.1124-70_1124-69insTCAGAG	XP_024303324.1:n.1124-70_1124-69insTCAGAG
XM_024447557.1:c.1124-70_1124-69insTCAGAG	XP_024303325.1:n.1124-70_1124-69insTCAGAG
XM_024447558.1:c.137-70_137-69insTCAGAG	XP_024303326.1:n.137-70_137-69insTCAGAG
XM_024447560.1:c.-285-70_-285-69insTCAGAG	XP_024303328.1:n.-285-70_-285-69insTCAGAG
XM_024447561.1:c.-285-70_-285-69insTCAGAG	XP_024303329.1:n.-285-70_-285-69insTCAGAG
NM_003995.4:c.1124-70_1124-69insTCAGAG MANE Select	NP_003986.2:n.1124-70_1124-69insTCAGAG
NM_001378923.1:c.1124-70_1124-69insTCAGAG	NP_001365852.1:n.1124-70_1124-69insTCAGAG