Canonical Allele Identifier: CA464615759

Gene: NPR2

Linked Data

• gnomAD v4: 9-35806180-A-C
• MyVariant Identifiers: chr9:g.35806177A>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806180A>C , CM000671.2:g.35806180A>C	GRCh38
NC_000009.11:g.35806177A>C , CM000671.1:g.35806177A>C	GRCh37
NC_000009.10:g.35796177A>C	NCBI36
NG_009249.1:g.18772A>C
NG_047141.1:g.11093T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.359A>C
ENST00000448821.6:c.2319A>C	ENSP00000402902.2:p.Pro773=
ENST00000685871.1:c.2247A>C	ENSP00000509964.1:p.Pro749=
ENST00000686159.1:n.2358A>C
ENST00000686486.1:n.1489A>C
ENST00000687302.1:n.2433A>C
ENST00000687357.1:c.2172A>C	ENSP00000509549.1:p.Pro724=
ENST00000687625.1:n.1474A>C
ENST00000687787.1:c.2478A>C	ENSP00000509440.1:p.Pro826=
ENST00000688201.1:n.2276A>C
ENST00000688226.1:n.2251A>C
ENST00000688869.1:n.2625A>C
ENST00000689788.1:c.2113A>C	ENSP00000508973.1:n.2113A>C
ENST00000689898.1:c.2176A>C	ENSP00000509651.1:n.2176A>C
ENST00000690070.1:c.2403A>C	ENSP00000509654.1:p.Pro801=
ENST00000690267.1:c.2108A>C	ENSP00000510432.1:n.2108A>C
ENST00000690552.1:n.2180A>C
ENST00000691138.1:n.2108A>C
ENST00000691969.1:c.1819A>C	ENSP00000510244.1:n.1819A>C
ENST00000692232.1:n.3634A>C
ENST00000692233.1:c.2183A>C	ENSP00000509698.1:n.2183A>C
ENST00000692380.1:n.1474A>C
ENST00000692447.1:n.3435A>C
ENST00000693094.1:c.2319A>C	ENSP00000510161.1:p.Pro773=
ENST00000342694.7:c.2319A>C MANE Select	ENSP00000341083.2:p.Pro773=
ENST00000342694.6:c.2319A>C	ENSP00000341083.2:p.Pro773=
ENST00000421267.5:c.359A>C
ENST00000447210.5:c.96A>C	ENSP00000393029.1:p.Pro32=
ENST00000464810.5:n.2319A>C
NM_003995.3:c.2319A>C	NP_003986.2:p.Pro773=
XM_005251478.3:c.2328A>C	XP_005251535.1:p.Pro776=
XM_005251479.3:c.1341A>C	XP_005251536.1:p.Pro447=
XM_006716778.2:c.2256A>C	XP_006716841.1:p.Pro752=
XM_011517889.1:c.1341A>C	XP_011516191.1:p.Pro447=
XM_011517890.1:c.1341A>C	XP_011516192.1:p.Pro447=
XM_011517891.1:c.1341A>C	XP_011516193.1:p.Pro447=
XM_011517892.1:c.1341A>C	XP_011516194.1:p.Pro447=
XM_011517893.1:c.1341A>C	XP_011516195.1:p.Pro447=
XM_011517894.1:c.1341A>C	XP_011516196.1:p.Pro447=
XM_011517895.1:c.924A>C	XP_011516197.1:p.Pro308=
XM_024447556.1:c.2487A>C	XP_024303324.1:p.Pro829=
XM_024447557.1:c.2478A>C	XP_024303325.1:p.Pro826=
XM_024447558.1:c.1500A>C	XP_024303326.1:p.Pro500=
XM_024447559.1:c.1083A>C	XP_024303327.1:p.Pro361=
XM_024447560.1:c.1074A>C	XP_024303328.1:p.Pro358=
XM_024447561.1:c.915A>C	XP_024303329.1:p.Pro305=
NM_003995.4:c.2319A>C MANE Select	NP_003986.2:p.Pro773=
NM_001378923.1:c.2328A>C	NP_001365852.1:p.Pro776=