Canonical Allele Identifier: CA459008261

Gene: VIPR2

Linked Data

• gnomAD v4: 7-159034587-G-C
• MyVariant Identifiers: chr7:g.158827278G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159034587G>C , CM000669.2:g.159034587G>C	GRCh38
NC_000007.13:g.158827278G>C , CM000669.1:g.158827278G>C	GRCh37
NC_000007.12:g.158520039G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.873C>G MANE Select	ENSP00000262178.2:p.Ser291=
ENST00000262178.6:c.873C>G	ENSP00000262178.2:p.Ser291=
ENST00000377633.7:c.825C>G	ENSP00000366860.3:p.Ser275=
ENST00000402066.5:c.1296C>G	ENSP00000384497.1:p.Ser432=
NM_001304522.1:c.633C>G	NP_001291451.1:p.Ser211=
NM_001308259.1:c.825C>G	NP_001295188.1:p.Ser275=
NM_003382.4:c.873C>G	NP_003373.2:p.Ser291=
NR_130758.1:n.1059C>G
XM_005249561.2:c.948C>G	XP_005249618.1:p.Ser316=
XM_006716107.1:c.873C>G	XP_006716170.1:p.Ser291=
XM_006716108.2:c.684C>G	XP_006716171.1:p.Ser228=
XM_011516550.1:c.825C>G	XP_011514852.1:p.Ser275=
XM_011516552.1:c.459C>G	XP_011514854.1:p.Ser153=
XR_242047.2:n.1268C>G
XM_005249561.3:c.948C>G	XP_005249618.1:p.Ser316=
XM_006716107.2:c.873C>G	XP_006716170.1:p.Ser291=
XM_006716108.3:c.684C>G	XP_006716171.1:p.Ser228=
XM_011516550.2:c.825C>G	XP_011514852.1:p.Ser275=
XM_017012580.1:c.459C>G	XP_016868069.1:p.Ser153=
XM_024446914.1:c.948C>G	XP_024302682.1:p.Ser316=
XM_024446915.1:c.948C>G	XP_024302683.1:p.Ser316=
XM_024446916.1:c.873C>G	XP_024302684.1:p.Ser291=
XM_024446917.1:c.684C>G	XP_024302685.1:p.Ser228=
XM_024446918.1:c.459C>G	XP_024302686.1:p.Ser153=
NM_003382.5:c.873C>G MANE Select	NP_003373.2:p.Ser291=
NM_001304522.2:c.633C>G	NP_001291451.1:p.Ser211=
NR_130758.2:n.969C>G