Canonical Allele Identifier: CA2685895298

Gene: VIPR2

Linked Data

• gnomAD v4: 7-159034420-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159034420A>G , CM000669.2:g.159034420A>G	GRCh38
NC_000007.13:g.158827111A>G , CM000669.1:g.158827111A>G	GRCh37
NC_000007.12:g.158519872A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.880-116T>C MANE Select	ENSP00000262178.2:n.880-116T>C
ENST00000262178.6:c.880-116T>C	ENSP00000262178.2:n.880-116T>C
ENST00000377633.7:c.832-116T>C	ENSP00000366860.3:n.832-116T>C
ENST00000402066.5:c.1303-116T>C	ENSP00000384497.1:n.1303-116T>C
NM_001304522.1:c.640-116T>C	NP_001291451.1:n.640-116T>C
NM_001308259.1:c.832-116T>C	NP_001295188.1:n.832-116T>C
NM_003382.4:c.880-116T>C	NP_003373.2:n.880-116T>C
NR_130758.1:n.1066-116T>C
XM_005249561.2:c.955-116T>C	XP_005249618.1:n.955-116T>C
XM_006716107.1:c.880-116T>C	XP_006716170.1:n.880-116T>C
XM_006716108.2:c.691-116T>C	XP_006716171.1:n.691-116T>C
XM_011516550.1:c.832-116T>C	XP_011514852.1:n.832-116T>C
XM_011516552.1:c.466-116T>C	XP_011514854.1:n.466-116T>C
XM_005249561.3:c.955-116T>C	XP_005249618.1:n.955-116T>C
XM_006716107.2:c.880-116T>C	XP_006716170.1:n.880-116T>C
XM_006716108.3:c.691-116T>C	XP_006716171.1:n.691-116T>C
XM_011516550.2:c.832-116T>C	XP_011514852.1:n.832-116T>C
XM_017012580.1:c.466-116T>C	XP_016868069.1:n.466-116T>C
XM_024446914.1:c.955-116T>C	XP_024302682.1:n.955-116T>C
XM_024446915.1:c.955-116T>C	XP_024302683.1:n.955-116T>C
XM_024446916.1:c.880-116T>C	XP_024302684.1:n.880-116T>C
XM_024446917.1:c.691-116T>C	XP_024302685.1:n.691-116T>C
XM_024446918.1:c.466-116T>C	XP_024302686.1:n.466-116T>C
NM_003382.5:c.880-116T>C MANE Select	NP_003373.2:n.880-116T>C
NM_001304522.2:c.640-116T>C	NP_001291451.1:n.640-116T>C
NR_130758.2:n.976-116T>C