Canonical Allele Identifier: CA369941493

Gene: VIPR2

Linked Data

• MyVariant Identifiers: chr7:g.158827321T>G (hg19) ; chr7:g.159034630T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159034630T>G , CM000669.2:g.159034630T>G	GRCh38
NC_000007.13:g.158827321T>G , CM000669.1:g.158827321T>G	GRCh37
NC_000007.12:g.158520082T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.830A>C MANE Select	ENSP00000262178.2:p.His277Pro
ENST00000262178.6:c.830A>C	ENSP00000262178.2:p.His277Pro
ENST00000377633.7:c.782A>C	ENSP00000366860.3:p.His261Pro
ENST00000402066.5:c.1253A>C	ENSP00000384497.1:p.His418Pro
NM_001304522.1:c.590A>C	NP_001291451.1:p.His197Pro
NM_001308259.1:c.782A>C	NP_001295188.1:p.His261Pro
NM_003382.4:c.830A>C	NP_003373.2:p.His277Pro
NR_130758.1:n.1016A>C
XM_005249561.2:c.905A>C	XP_005249618.1:p.His302Pro
XM_006716107.1:c.830A>C	XP_006716170.1:p.His277Pro
XM_006716108.2:c.641A>C	XP_006716171.1:p.His214Pro
XM_011516550.1:c.782A>C	XP_011514852.1:p.His261Pro
XM_011516552.1:c.416A>C	XP_011514854.1:p.His139Pro
XR_242047.2:n.1225A>C
XM_005249561.3:c.905A>C	XP_005249618.1:p.His302Pro
XM_006716107.2:c.830A>C	XP_006716170.1:p.His277Pro
XM_006716108.3:c.641A>C	XP_006716171.1:p.His214Pro
XM_011516550.2:c.782A>C	XP_011514852.1:p.His261Pro
XM_017012580.1:c.416A>C	XP_016868069.1:p.His139Pro
XM_024446914.1:c.905A>C	XP_024302682.1:p.His302Pro
XM_024446915.1:c.905A>C	XP_024302683.1:p.His302Pro
XM_024446916.1:c.830A>C	XP_024302684.1:p.His277Pro
XM_024446917.1:c.641A>C	XP_024302685.1:p.His214Pro
XM_024446918.1:c.416A>C	XP_024302686.1:p.His139Pro
NM_003382.5:c.830A>C MANE Select	NP_003373.2:p.His277Pro
NM_001304522.2:c.590A>C	NP_001291451.1:p.His197Pro
NR_130758.2:n.926A>C