Canonical Allele Identifier: CA373379103

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806153G>T (hg19) ; chr9:g.35806156G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806156G>T , CM000671.2:g.35806156G>T	GRCh38
NC_000009.11:g.35806153G>T , CM000671.1:g.35806153G>T	GRCh37
NC_000009.10:g.35796153G>T	NCBI36
NG_009249.1:g.18748G>T
NG_047141.1:g.11117C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.335G>T
ENST00000448821.6:c.2295G>T	ENSP00000402902.2:p.Met765Ile
ENST00000685871.1:c.2223G>T	ENSP00000509964.1:p.Met741Ile
ENST00000686159.1:n.2334G>T
ENST00000686486.1:n.1465G>T
ENST00000687302.1:n.2409G>T
ENST00000687357.1:c.2148G>T	ENSP00000509549.1:p.Met716Ile
ENST00000687625.1:n.1450G>T
ENST00000687787.1:c.2454G>T	ENSP00000509440.1:p.Met818Ile
ENST00000688201.1:n.2252G>T
ENST00000688226.1:n.2227G>T
ENST00000688869.1:n.2601G>T
ENST00000689788.1:c.2089G>T	ENSP00000508973.1:n.2089G>T
ENST00000689898.1:c.2152G>T	ENSP00000509651.1:n.2152G>T
ENST00000690070.1:c.2379G>T	ENSP00000509654.1:p.Met793Ile
ENST00000690267.1:c.2084G>T	ENSP00000510432.1:n.2084G>T
ENST00000690552.1:n.2156G>T
ENST00000691138.1:n.2084G>T
ENST00000691969.1:c.1795G>T	ENSP00000510244.1:n.1795G>T
ENST00000692232.1:n.3610G>T
ENST00000692233.1:c.2159G>T	ENSP00000509698.1:n.2159G>T
ENST00000692380.1:n.1450G>T
ENST00000692447.1:n.3411G>T
ENST00000693094.1:c.2295G>T	ENSP00000510161.1:p.Met765Ile
ENST00000342694.7:c.2295G>T MANE Select	ENSP00000341083.2:p.Met765Ile
ENST00000342694.6:c.2295G>T	ENSP00000341083.2:p.Met765Ile
ENST00000421267.5:c.335G>T
ENST00000447210.5:c.72G>T	ENSP00000393029.1:p.Met24Ile
ENST00000464810.5:n.2295G>T
NM_003995.3:c.2295G>T	NP_003986.2:p.Met765Ile
XM_005251478.3:c.2304G>T	XP_005251535.1:p.Met768Ile
XM_005251479.3:c.1317G>T	XP_005251536.1:p.Met439Ile
XM_006716778.2:c.2232G>T	XP_006716841.1:p.Met744Ile
XM_011517889.1:c.1317G>T	XP_011516191.1:p.Met439Ile
XM_011517890.1:c.1317G>T	XP_011516192.1:p.Met439Ile
XM_011517891.1:c.1317G>T	XP_011516193.1:p.Met439Ile
XM_011517892.1:c.1317G>T	XP_011516194.1:p.Met439Ile
XM_011517893.1:c.1317G>T	XP_011516195.1:p.Met439Ile
XM_011517894.1:c.1317G>T	XP_011516196.1:p.Met439Ile
XM_011517895.1:c.900G>T	XP_011516197.1:p.Met300Ile
XM_024447556.1:c.2463G>T	XP_024303324.1:p.Met821Ile
XM_024447557.1:c.2454G>T	XP_024303325.1:p.Met818Ile
XM_024447558.1:c.1476G>T	XP_024303326.1:p.Met492Ile
XM_024447559.1:c.1059G>T	XP_024303327.1:p.Met353Ile
XM_024447560.1:c.1050G>T	XP_024303328.1:p.Met350Ile
XM_024447561.1:c.891G>T	XP_024303329.1:p.Met297Ile
NM_003995.4:c.2295G>T MANE Select	NP_003986.2:p.Met765Ile
NM_001378923.1:c.2304G>T	NP_001365852.1:p.Met768Ile