Canonical Allele Identifier: CA2689904835

Gene: NPR2

Linked Data

• gnomAD v4: 9-35800736-AAGC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35800739_35800741del , CM000671.2:g.35800739_35800741del	GRCh38
NC_000009.11:g.35800736_35800738del , CM000671.1:g.35800736_35800738del	GRCh37
NC_000009.10:g.35790736_35790738del	NCBI36
NG_009249.1:g.13331_13333del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000448821.6:c.1249_1251del	ENSP00000402902.2:p.Gln417del
ENST00000685871.1:c.1249_1251del	ENSP00000509964.1:p.Gln417del
ENST00000686159.1:n.1288_1290del
ENST00000686486.1:n.257_259del
ENST00000687302.1:n.1335_1337del
ENST00000687357.1:c.1249_1251del	ENSP00000509549.1:p.Gln417del
ENST00000687625.1:n.404_406del
ENST00000687787.1:c.1249_1251del	ENSP00000509440.1:p.Gln417del
ENST00000688201.1:n.1281_1283del
ENST00000688226.1:n.1181_1183del
ENST00000688869.1:n.1555_1557del
ENST00000689788.1:c.1043_1045del	ENSP00000508973.1:n.1043_1045del
ENST00000689898.1:c.1249_1251del	ENSP00000509651.1:p.Gln417del
ENST00000690070.1:c.1249_1251del	ENSP00000509654.1:p.Gln417del
ENST00000690267.1:c.1113_1115del	ENSP00000510432.1:n.1113_1115del
ENST00000690552.1:n.1110_1112del
ENST00000691138.1:n.1110_1112del
ENST00000691969.1:c.824_826del	ENSP00000510244.1:n.824_826del
ENST00000692232.1:n.2405_2407del
ENST00000692233.1:c.1113_1115del	ENSP00000509698.1:n.1113_1115del
ENST00000692380.1:n.404_406del
ENST00000692447.1:n.2361_2363del
ENST00000693094.1:c.1249_1251del	ENSP00000510161.1:p.Gln417del
ENST00000342694.7:c.1249_1251del MANE Select	ENSP00000341083.2:p.Gln417del
ENST00000342694.6:c.1249_1251del	ENSP00000341083.2:p.Gln417del
ENST00000464810.5:n.1249_1251del
NM_003995.3:c.1249_1251del	NP_003986.2:p.Gln417del
XM_005251478.3:c.1249_1251del	XP_005251535.1:p.Gln417del
XM_005251479.3:c.262_264del	XP_005251536.1:p.Gln88del
XM_006716778.2:c.1249_1251del	XP_006716841.1:p.Gln417del
XM_011517889.1:c.262_264del	XP_011516191.1:p.Gln88del
XM_011517890.1:c.262_264del	XP_011516192.1:p.Gln88del
XM_011517891.1:c.262_264del	XP_011516193.1:p.Gln88del
XM_011517892.1:c.262_264del	XP_011516194.1:p.Gln88del
XM_011517893.1:c.262_264del	XP_011516195.1:p.Gln88del
XM_011517894.1:c.262_264del	XP_011516196.1:p.Gln88del
XM_024447556.1:c.1249_1251del	XP_024303324.1:p.Gln417del
XM_024447557.1:c.1249_1251del	XP_024303325.1:p.Gln417del
XM_024447558.1:c.262_264del	XP_024303326.1:p.Gln88del
XM_024447560.1:c.-160_-158del	XP_024303328.1:n.-160_-158del
XM_024447561.1:c.-160_-158del	XP_024303329.1:n.-160_-158del
NM_003995.4:c.1249_1251del MANE Select	NP_003986.2:p.Gln417del
NM_001378923.1:c.1249_1251del	NP_001365852.1:p.Gln417del