Canonical Allele Identifier: CA369940842

Gene: VIPR2

Linked Data

• gnomAD v4: 7-159034303-A-T
• MyVariant Identifiers: chr7:g.158826994A>T (hg19) ; chr7:g.159034303A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159034303A>T , CM000669.2:g.159034303A>T	GRCh38
NC_000007.13:g.158826994A>T , CM000669.1:g.158826994A>T	GRCh37
NC_000007.12:g.158519755A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.881T>A MANE Select	ENSP00000262178.2:p.Val294Asp
ENST00000262178.6:c.881T>A	ENSP00000262178.2:p.Val294Asp
ENST00000377633.7:c.833T>A	ENSP00000366860.3:p.Val278Asp
ENST00000402066.5:c.1304T>A	ENSP00000384497.1:p.Val435Asp
NM_001304522.1:c.641T>A	NP_001291451.1:p.Val214Asp
NM_001308259.1:c.833T>A	NP_001295188.1:p.Val278Asp
NM_003382.4:c.881T>A	NP_003373.2:p.Val294Asp
NR_130758.1:n.1067T>A
XM_005249561.2:c.956T>A	XP_005249618.1:p.Val319Asp
XM_006716107.1:c.881T>A	XP_006716170.1:p.Val294Asp
XM_006716108.2:c.692T>A	XP_006716171.1:p.Val231Asp
XM_011516550.1:c.833T>A	XP_011514852.1:p.Val278Asp
XM_011516552.1:c.467T>A	XP_011514854.1:p.Val156Asp
XM_005249561.3:c.956T>A	XP_005249618.1:p.Val319Asp
XM_006716107.2:c.881T>A	XP_006716170.1:p.Val294Asp
XM_006716108.3:c.692T>A	XP_006716171.1:p.Val231Asp
XM_011516550.2:c.833T>A	XP_011514852.1:p.Val278Asp
XM_017012580.1:c.467T>A	XP_016868069.1:p.Val156Asp
XM_024446914.1:c.956T>A	XP_024302682.1:p.Val319Asp
XM_024446915.1:c.956T>A	XP_024302683.1:p.Val319Asp
XM_024446916.1:c.881T>A	XP_024302684.1:p.Val294Asp
XM_024446917.1:c.692T>A	XP_024302685.1:p.Val231Asp
XM_024446918.1:c.467T>A	XP_024302686.1:p.Val156Asp
NM_003382.5:c.881T>A MANE Select	NP_003373.2:p.Val294Asp
NM_001304522.2:c.641T>A	NP_001291451.1:p.Val214Asp
NR_130758.2:n.977T>A