Canonical Allele Identifier: CA369941238

Gene: VIPR2

Linked Data

• MyVariant Identifiers: chr7:g.158827294A>G (hg19) ; chr7:g.159034603A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159034603A>G , CM000669.2:g.159034603A>G	GRCh38
NC_000007.13:g.158827294A>G , CM000669.1:g.158827294A>G	GRCh37
NC_000007.12:g.158520055A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.857T>C MANE Select	ENSP00000262178.2:p.Ile286Thr
ENST00000262178.6:c.857T>C	ENSP00000262178.2:p.Ile286Thr
ENST00000377633.7:c.809T>C	ENSP00000366860.3:p.Ile270Thr
ENST00000402066.5:c.1280T>C	ENSP00000384497.1:p.Ile427Thr
NM_001304522.1:c.617T>C	NP_001291451.1:p.Ile206Thr
NM_001308259.1:c.809T>C	NP_001295188.1:p.Ile270Thr
NM_003382.4:c.857T>C	NP_003373.2:p.Ile286Thr
NR_130758.1:n.1043T>C
XM_005249561.2:c.932T>C	XP_005249618.1:p.Ile311Thr
XM_006716107.1:c.857T>C	XP_006716170.1:p.Ile286Thr
XM_006716108.2:c.668T>C	XP_006716171.1:p.Ile223Thr
XM_011516550.1:c.809T>C	XP_011514852.1:p.Ile270Thr
XM_011516552.1:c.443T>C	XP_011514854.1:p.Ile148Thr
XR_242047.2:n.1252T>C
XM_005249561.3:c.932T>C	XP_005249618.1:p.Ile311Thr
XM_006716107.2:c.857T>C	XP_006716170.1:p.Ile286Thr
XM_006716108.3:c.668T>C	XP_006716171.1:p.Ile223Thr
XM_011516550.2:c.809T>C	XP_011514852.1:p.Ile270Thr
XM_017012580.1:c.443T>C	XP_016868069.1:p.Ile148Thr
XM_024446914.1:c.932T>C	XP_024302682.1:p.Ile311Thr
XM_024446915.1:c.932T>C	XP_024302683.1:p.Ile311Thr
XM_024446916.1:c.857T>C	XP_024302684.1:p.Ile286Thr
XM_024446917.1:c.668T>C	XP_024302685.1:p.Ile223Thr
XM_024446918.1:c.443T>C	XP_024302686.1:p.Ile148Thr
NM_003382.5:c.857T>C MANE Select	NP_003373.2:p.Ile286Thr
NM_001304522.2:c.617T>C	NP_001291451.1:p.Ile206Thr
NR_130758.2:n.953T>C