Canonical Allele Identifier: CA369941514

Gene: VIPR2

Linked Data

• MyVariant Identifiers: chr7:g.158827325C>G (hg19) ; chr7:g.159034634C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159034634C>G , CM000669.2:g.159034634C>G	GRCh38
NC_000007.13:g.158827325C>G , CM000669.1:g.158827325C>G	GRCh37
NC_000007.12:g.158520086C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.826G>C MANE Select	ENSP00000262178.2:p.Asp276His
ENST00000262178.6:c.826G>C	ENSP00000262178.2:p.Asp276His
ENST00000377633.7:c.778G>C	ENSP00000366860.3:p.Asp260His
ENST00000402066.5:c.1249G>C	ENSP00000384497.1:p.Asp417His
NM_001304522.1:c.586G>C	NP_001291451.1:p.Asp196His
NM_001308259.1:c.778G>C	NP_001295188.1:p.Asp260His
NM_003382.4:c.826G>C	NP_003373.2:p.Asp276His
NR_130758.1:n.1012G>C
XM_005249561.2:c.901G>C	XP_005249618.1:p.Asp301His
XM_006716107.1:c.826G>C	XP_006716170.1:p.Asp276His
XM_006716108.2:c.637G>C	XP_006716171.1:p.Asp213His
XM_011516550.1:c.778G>C	XP_011514852.1:p.Asp260His
XM_011516552.1:c.412G>C	XP_011514854.1:p.Asp138His
XR_242047.2:n.1221G>C
XM_005249561.3:c.901G>C	XP_005249618.1:p.Asp301His
XM_006716107.2:c.826G>C	XP_006716170.1:p.Asp276His
XM_006716108.3:c.637G>C	XP_006716171.1:p.Asp213His
XM_011516550.2:c.778G>C	XP_011514852.1:p.Asp260His
XM_017012580.1:c.412G>C	XP_016868069.1:p.Asp138His
XM_024446914.1:c.901G>C	XP_024302682.1:p.Asp301His
XM_024446915.1:c.901G>C	XP_024302683.1:p.Asp301His
XM_024446916.1:c.826G>C	XP_024302684.1:p.Asp276His
XM_024446917.1:c.637G>C	XP_024302685.1:p.Asp213His
XM_024446918.1:c.412G>C	XP_024302686.1:p.Asp138His
NM_003382.5:c.826G>C MANE Select	NP_003373.2:p.Asp276His
NM_001304522.2:c.586G>C	NP_001291451.1:p.Asp196His
NR_130758.2:n.922G>C