Canonical Allele Identifier: CA588146129

Gene: NPR2

Linked Data

• dbSNP Id: rs1313911223
• gnomAD v2: 9-35792509-ACCTGAGCTATG-A
• gnomAD v4: 9-35792512-ACCTGAGCTATG-A
• MyVariant Identifiers: chr9:g.35792510_35792520del (hg19) ; chr9:g.35792513_35792523del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35792517_35792527del , CM000671.2:g.35792517_35792527del	GRCh38
NC_000009.11:g.35792514_35792524del , CM000671.1:g.35792514_35792524del	GRCh37
NC_000009.10:g.35782514_35782524del	NCBI36
NG_009249.1:g.5109_5119del

Transcript Alleles

HGVS	Amino-acid change
ENST00000448821.6:c.109_119del	ENSP00000402902.2:p.Ser37GlyfsTer?
ENST00000685871.1:c.109_119del	ENSP00000509964.1:p.Ser37GlyfsTer?
ENST00000686159.1:n.148_158del
ENST00000687357.1:c.109_119del	ENSP00000509549.1:p.Ser37GlyfsTer?
ENST00000687625.1:n.164+1351_164+1361del
ENST00000687787.1:c.109_119del	ENSP00000509440.1:p.Ser37GlyfsTer?
ENST00000688201.1:n.141_151del
ENST00000688869.1:n.190_200del
ENST00000689788.1:c.109_119del	ENSP00000508973.1:p.Ser37GlyfsTer?
ENST00000689898.1:c.109_119del	ENSP00000509651.1:p.Ser37GlyfsTer?
ENST00000690070.1:c.109_119del	ENSP00000509654.1:p.Ser37GlyfsTer?
ENST00000690267.1:c.109_119del	ENSP00000510432.1:p.Ser37GlyfsTer?
ENST00000691969.1:c.109_119del	ENSP00000510244.1:p.Ser37GlyfsTer?
ENST00000692233.1:c.109_119del	ENSP00000509698.1:p.Ser37GlyfsTer?
ENST00000692380.1:n.164+1351_164+1361del
ENST00000692447.1:n.109_119del
ENST00000693094.1:c.109_119del	ENSP00000510161.1:p.Ser37GlyfsTer?
ENST00000342694.7:c.109_119del MANE Select	ENSP00000341083.2:p.Ser37GlyfsTer?
ENST00000342694.6:c.109_119del	ENSP00000341083.2:p.Ser37GlyfsTer?
ENST00000464810.5:n.109_119del
NM_003995.3:c.109_119del	NP_003986.2:p.Ser37GlyfsTer?
XM_005251478.3:c.109_119del	XP_005251535.1:p.Ser37GlyfsTer?
XM_005251479.3:c.-115+2177_-115+2187del	XP_005251536.1:n.-115+2177_-115+2187del
XM_006716778.2:c.109_119del	XP_006716841.1:p.Ser37GlyfsTer?
XM_011517889.1:c.-115+2177_-115+2187del	XP_011516191.1:n.-115+2177_-115+2187del
XM_011517890.1:c.-115+2177_-115+2187del	XP_011516192.1:n.-115+2177_-115+2187del
XM_011517891.1:c.-115+2177_-115+2187del	XP_011516193.1:n.-115+2177_-115+2187del
XM_011517892.1:c.-115+2177_-115+2187del	XP_011516194.1:n.-115+2177_-115+2187del
XM_011517893.1:c.-115+2177_-115+2187del	XP_011516195.1:n.-115+2177_-115+2187del
XM_011517894.1:c.-115+2177_-115+2187del	XP_011516196.1:n.-115+2177_-115+2187del
XM_024447556.1:c.109_119del	XP_024303324.1:p.Ser37GlyfsTer?
XM_024447557.1:c.109_119del	XP_024303325.1:p.Ser37GlyfsTer?
XM_024447558.1:c.-115+2177_-115+2187del	XP_024303326.1:n.-115+2177_-115+2187del
NM_003995.4:c.109_119del MANE Select	NP_003986.2:p.Ser37GlyfsTer?
NM_001378923.1:c.109_119del	NP_001365852.1:p.Ser37GlyfsTer?