Canonical Allele Identifier: CA373379162

Gene: NPR2

Linked Data

• MyVariant Identifiers: chr9:g.35806164G>T (hg19) ; chr9:g.35806167G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35806167G>T , CM000671.2:g.35806167G>T	GRCh38
NC_000009.11:g.35806164G>T , CM000671.1:g.35806164G>T	GRCh37
NC_000009.10:g.35796164G>T	NCBI36
NG_009249.1:g.18759G>T
NG_047141.1:g.11106C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000421267.6:c.346G>T
ENST00000448821.6:c.2306G>T	ENSP00000402902.2:p.Trp769Leu
ENST00000685871.1:c.2234G>T	ENSP00000509964.1:p.Trp745Leu
ENST00000686159.1:n.2345G>T
ENST00000686486.1:n.1476G>T
ENST00000687302.1:n.2420G>T
ENST00000687357.1:c.2159G>T	ENSP00000509549.1:p.Trp720Leu
ENST00000687625.1:n.1461G>T
ENST00000687787.1:c.2465G>T	ENSP00000509440.1:p.Trp822Leu
ENST00000688201.1:n.2263G>T
ENST00000688226.1:n.2238G>T
ENST00000688869.1:n.2612G>T
ENST00000689788.1:c.2100G>T	ENSP00000508973.1:n.2100G>T
ENST00000689898.1:c.2163G>T	ENSP00000509651.1:n.2163G>T
ENST00000690070.1:c.2390G>T	ENSP00000509654.1:p.Trp797Leu
ENST00000690267.1:c.2095G>T	ENSP00000510432.1:n.2095G>T
ENST00000690552.1:n.2167G>T
ENST00000691138.1:n.2095G>T
ENST00000691969.1:c.1806G>T	ENSP00000510244.1:n.1806G>T
ENST00000692232.1:n.3621G>T
ENST00000692233.1:c.2170G>T	ENSP00000509698.1:n.2170G>T
ENST00000692380.1:n.1461G>T
ENST00000692447.1:n.3422G>T
ENST00000693094.1:c.2306G>T	ENSP00000510161.1:p.Trp769Leu
ENST00000342694.7:c.2306G>T MANE Select	ENSP00000341083.2:p.Trp769Leu
ENST00000342694.6:c.2306G>T	ENSP00000341083.2:p.Trp769Leu
ENST00000421267.5:c.346G>T
ENST00000447210.5:c.83G>T	ENSP00000393029.1:p.Trp28Leu
ENST00000464810.5:n.2306G>T
NM_003995.3:c.2306G>T	NP_003986.2:p.Trp769Leu
XM_005251478.3:c.2315G>T	XP_005251535.1:p.Trp772Leu
XM_005251479.3:c.1328G>T	XP_005251536.1:p.Trp443Leu
XM_006716778.2:c.2243G>T	XP_006716841.1:p.Trp748Leu
XM_011517889.1:c.1328G>T	XP_011516191.1:p.Trp443Leu
XM_011517890.1:c.1328G>T	XP_011516192.1:p.Trp443Leu
XM_011517891.1:c.1328G>T	XP_011516193.1:p.Trp443Leu
XM_011517892.1:c.1328G>T	XP_011516194.1:p.Trp443Leu
XM_011517893.1:c.1328G>T	XP_011516195.1:p.Trp443Leu
XM_011517894.1:c.1328G>T	XP_011516196.1:p.Trp443Leu
XM_011517895.1:c.911G>T	XP_011516197.1:p.Trp304Leu
XM_024447556.1:c.2474G>T	XP_024303324.1:p.Trp825Leu
XM_024447557.1:c.2465G>T	XP_024303325.1:p.Trp822Leu
XM_024447558.1:c.1487G>T	XP_024303326.1:p.Trp496Leu
XM_024447559.1:c.1070G>T	XP_024303327.1:p.Trp357Leu
XM_024447560.1:c.1061G>T	XP_024303328.1:p.Trp354Leu
XM_024447561.1:c.902G>T	XP_024303329.1:p.Trp301Leu
NM_003995.4:c.2306G>T MANE Select	NP_003986.2:p.Trp769Leu
NM_001378923.1:c.2315G>T	NP_001365852.1:p.Trp772Leu