Canonical Allele Identifier: CA369941128

Gene: VIPR2

Linked Data

• MyVariant Identifiers: chr7:g.158827281A>C (hg19) ; chr7:g.159034590A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159034590A>C , CM000669.2:g.159034590A>C	GRCh38
NC_000007.13:g.158827281A>C , CM000669.1:g.158827281A>C	GRCh37
NC_000007.12:g.158520042A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.870T>G MANE Select	ENSP00000262178.2:p.Ile290Met
ENST00000262178.6:c.870T>G	ENSP00000262178.2:p.Ile290Met
ENST00000377633.7:c.822T>G	ENSP00000366860.3:p.Ile274Met
ENST00000402066.5:c.1293T>G	ENSP00000384497.1:p.Ile431Met
NM_001304522.1:c.630T>G	NP_001291451.1:p.Ile210Met
NM_001308259.1:c.822T>G	NP_001295188.1:p.Ile274Met
NM_003382.4:c.870T>G	NP_003373.2:p.Ile290Met
NR_130758.1:n.1056T>G
XM_005249561.2:c.945T>G	XP_005249618.1:p.Ile315Met
XM_006716107.1:c.870T>G	XP_006716170.1:p.Ile290Met
XM_006716108.2:c.681T>G	XP_006716171.1:p.Ile227Met
XM_011516550.1:c.822T>G	XP_011514852.1:p.Ile274Met
XM_011516552.1:c.456T>G	XP_011514854.1:p.Ile152Met
XR_242047.2:n.1265T>G
XM_005249561.3:c.945T>G	XP_005249618.1:p.Ile315Met
XM_006716107.2:c.870T>G	XP_006716170.1:p.Ile290Met
XM_006716108.3:c.681T>G	XP_006716171.1:p.Ile227Met
XM_011516550.2:c.822T>G	XP_011514852.1:p.Ile274Met
XM_017012580.1:c.456T>G	XP_016868069.1:p.Ile152Met
XM_024446914.1:c.945T>G	XP_024302682.1:p.Ile315Met
XM_024446915.1:c.945T>G	XP_024302683.1:p.Ile315Met
XM_024446916.1:c.870T>G	XP_024302684.1:p.Ile290Met
XM_024446917.1:c.681T>G	XP_024302685.1:p.Ile227Met
XM_024446918.1:c.456T>G	XP_024302686.1:p.Ile152Met
NM_003382.5:c.870T>G MANE Select	NP_003373.2:p.Ile290Met
NM_001304522.2:c.630T>G	NP_001291451.1:p.Ile210Met
NR_130758.2:n.966T>G