Canonical Allele Identifier: CA2689906047

Gene: NPR2

Linked Data

• gnomAD v4: 9-35801233-T-TCCCACGTTATAGGG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35801233_35801234insCCCACGTTATAGGG , CM000671.2:g.35801233_35801234insCCCACGTTATAGGG	GRCh38
NC_000009.11:g.35801230_35801231insCCCACGTTATAGGG , CM000671.1:g.35801230_35801231insCCCACGTTATAGGG	GRCh37
NC_000009.10:g.35791230_35791231insCCCACGTTATAGGG	NCBI36
NG_009249.1:g.13825_13826insCCCACGTTATAGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448821.6:c.1436+79_1436+80insCCCACGTTATAGGG	ENSP00000402902.2:n.1436+79_1436+80insCCCACGTTATAGGG
ENST00000685871.1:c.1436+79_1436+80insCCCACGTTATAGGG	ENSP00000509964.1:n.1436+79_1436+80insCCCACGTTATAGGG
ENST00000686159.1:n.1475+79_1475+80insCCCACGTTATAGGG
ENST00000686486.1:n.444+79_444+80insCCCACGTTATAGGG
ENST00000687302.1:n.1522+79_1522+80insCCCACGTTATAGGG
ENST00000687357.1:c.1436+79_1436+80insCCCACGTTATAGGG	ENSP00000509549.1:n.1436+79_1436+80insCCCACGTTATAGGG
ENST00000687625.1:n.591+79_591+80insCCCACGTTATAGGG
ENST00000687787.1:c.1436+79_1436+80insCCCACGTTATAGGG	ENSP00000509440.1:n.1436+79_1436+80insCCCACGTTATAGGG
ENST00000688201.1:n.1468+79_1468+80insCCCACGTTATAGGG
ENST00000688226.1:n.1368+79_1368+80insCCCACGTTATAGGG
ENST00000688869.1:n.1742+79_1742+80insCCCACGTTATAGGG
ENST00000689788.1:c.1230+79_1230+80insCCCACGTTATAGGG	ENSP00000508973.1:n.1230+79_1230+80insCCCACGTTATAGGG
ENST00000689898.1:c.1440+79_1440+80insCCCACGTTATAGGG	ENSP00000509651.1:n.1440+79_1440+80insCCCACGTTATAGGG
ENST00000690070.1:c.1436+79_1436+80insCCCACGTTATAGGG	ENSP00000509654.1:n.1436+79_1436+80insCCCACGTTATAGGG
ENST00000690267.1:c.1300+79_1300+80insCCCACGTTATAGGG	ENSP00000510432.1:n.1300+79_1300+80insCCCACGTTATAGGG
ENST00000690552.1:n.1297+79_1297+80insCCCACGTTATAGGG
ENST00000691138.1:n.1297+79_1297+80insCCCACGTTATAGGG
ENST00000691969.1:c.1011+79_1011+80insCCCACGTTATAGGG	ENSP00000510244.1:n.1011+79_1011+80insCCCACGTTATAGGG
ENST00000692232.1:n.2592+79_2592+80insCCCACGTTATAGGG
ENST00000692233.1:c.1300+79_1300+80insCCCACGTTATAGGG	ENSP00000509698.1:n.1300+79_1300+80insCCCACGTTATAGGG
ENST00000692380.1:n.591+79_591+80insCCCACGTTATAGGG
ENST00000692447.1:n.2552+79_2552+80insCCCACGTTATAGGG
ENST00000693094.1:c.1436+79_1436+80insCCCACGTTATAGGG	ENSP00000510161.1:n.1436+79_1436+80insCCCACGTTATAGGG
ENST00000342694.7:c.1436+79_1436+80insCCCACGTTATAGGG MANE Select	ENSP00000341083.2:n.1436+79_1436+80insCCCACGTTATAGGG
ENST00000342694.6:c.1436+79_1436+80insCCCACGTTATAGGG	ENSP00000341083.2:n.1436+79_1436+80insCCCACGTTATAGGG
ENST00000464810.5:n.1436+79_1436+80insCCCACGTTATAGGG
NM_003995.3:c.1436+79_1436+80insCCCACGTTATAGGG	NP_003986.2:n.1436+79_1436+80insCCCACGTTATAGGG
XM_005251478.3:c.1436+79_1436+80insCCCACGTTATAGGG	XP_005251535.1:n.1436+79_1436+80insCCCACGTTATAGGG
XM_005251479.3:c.449+79_449+80insCCCACGTTATAGGG	XP_005251536.1:n.449+79_449+80insCCCACGTTATAGGG
XM_006716778.2:c.1436+79_1436+80insCCCACGTTATAGGG	XP_006716841.1:n.1436+79_1436+80insCCCACGTTATAGGG
XM_011517889.1:c.449+79_449+80insCCCACGTTATAGGG	XP_011516191.1:n.449+79_449+80insCCCACGTTATAGGG
XM_011517890.1:c.449+79_449+80insCCCACGTTATAGGG	XP_011516192.1:n.449+79_449+80insCCCACGTTATAGGG
XM_011517891.1:c.449+79_449+80insCCCACGTTATAGGG	XP_011516193.1:n.449+79_449+80insCCCACGTTATAGGG
XM_011517892.1:c.449+79_449+80insCCCACGTTATAGGG	XP_011516194.1:n.449+79_449+80insCCCACGTTATAGGG
XM_011517893.1:c.449+79_449+80insCCCACGTTATAGGG	XP_011516195.1:n.449+79_449+80insCCCACGTTATAGGG
XM_011517894.1:c.449+79_449+80insCCCACGTTATAGGG	XP_011516196.1:n.449+79_449+80insCCCACGTTATAGGG
XM_011517895.1:c.32+79_32+80insCCCACGTTATAGGG	XP_011516197.1:n.32+79_32+80insCCCACGTTATAGGG
XM_024447556.1:c.1436+79_1436+80insCCCACGTTATAGGG	XP_024303324.1:n.1436+79_1436+80insCCCACGTTATAGGG
XM_024447557.1:c.1436+79_1436+80insCCCACGTTATAGGG	XP_024303325.1:n.1436+79_1436+80insCCCACGTTATAGGG
XM_024447558.1:c.449+79_449+80insCCCACGTTATAGGG	XP_024303326.1:n.449+79_449+80insCCCACGTTATAGGG
XM_024447559.1:c.32+79_32+80insCCCACGTTATAGGG	XP_024303327.1:n.32+79_32+80insCCCACGTTATAGGG
XM_024447560.1:c.32+79_32+80insCCCACGTTATAGGG	XP_024303328.1:n.32+79_32+80insCCCACGTTATAGGG
XM_024447561.1:c.32+79_32+80insCCCACGTTATAGGG	XP_024303329.1:n.32+79_32+80insCCCACGTTATAGGG
NM_003995.4:c.1436+79_1436+80insCCCACGTTATAGGG MANE Select	NP_003986.2:n.1436+79_1436+80insCCCACGTTATAGGG
NM_001378923.1:c.1436+79_1436+80insCCCACGTTATAGGG	NP_001365852.1:n.1436+79_1436+80insCCCACGTTATAGGG