Canonical Allele Identifier: CA369941484

Gene: VIPR2

Linked Data

• MyVariant Identifiers: chr7:g.158827320G>T (hg19) ; chr7:g.159034629G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159034629G>T , CM000669.2:g.159034629G>T	GRCh38
NC_000007.13:g.158827320G>T , CM000669.1:g.158827320G>T	GRCh37
NC_000007.12:g.158520081G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.831C>A MANE Select	ENSP00000262178.2:p.His277Gln
ENST00000262178.6:c.831C>A	ENSP00000262178.2:p.His277Gln
ENST00000377633.7:c.783C>A	ENSP00000366860.3:p.His261Gln
ENST00000402066.5:c.1254C>A	ENSP00000384497.1:p.His418Gln
NM_001304522.1:c.591C>A	NP_001291451.1:p.His197Gln
NM_001308259.1:c.783C>A	NP_001295188.1:p.His261Gln
NM_003382.4:c.831C>A	NP_003373.2:p.His277Gln
NR_130758.1:n.1017C>A
XM_005249561.2:c.906C>A	XP_005249618.1:p.His302Gln
XM_006716107.1:c.831C>A	XP_006716170.1:p.His277Gln
XM_006716108.2:c.642C>A	XP_006716171.1:p.His214Gln
XM_011516550.1:c.783C>A	XP_011514852.1:p.His261Gln
XM_011516552.1:c.417C>A	XP_011514854.1:p.His139Gln
XR_242047.2:n.1226C>A
XM_005249561.3:c.906C>A	XP_005249618.1:p.His302Gln
XM_006716107.2:c.831C>A	XP_006716170.1:p.His277Gln
XM_006716108.3:c.642C>A	XP_006716171.1:p.His214Gln
XM_011516550.2:c.783C>A	XP_011514852.1:p.His261Gln
XM_017012580.1:c.417C>A	XP_016868069.1:p.His139Gln
XM_024446914.1:c.906C>A	XP_024302682.1:p.His302Gln
XM_024446915.1:c.906C>A	XP_024302683.1:p.His302Gln
XM_024446916.1:c.831C>A	XP_024302684.1:p.His277Gln
XM_024446917.1:c.642C>A	XP_024302685.1:p.His214Gln
XM_024446918.1:c.417C>A	XP_024302686.1:p.His139Gln
NM_003382.5:c.831C>A MANE Select	NP_003373.2:p.His277Gln
NM_001304522.2:c.591C>A	NP_001291451.1:p.His197Gln
NR_130758.2:n.927C>A