Canonical Allele Identifier: CA2507748447

Gene: VIPR2

Linked Data

• gnomAD v4: 7-159034317-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159034317T>C , CM000669.2:g.159034317T>C	GRCh38
NC_000007.13:g.158827008T>C , CM000669.1:g.158827008T>C	GRCh37
NC_000007.12:g.158519769T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.880-13A>G MANE Select	ENSP00000262178.2:n.880-13A>G
ENST00000262178.6:c.880-13A>G	ENSP00000262178.2:n.880-13A>G
ENST00000377633.7:c.832-13A>G	ENSP00000366860.3:n.832-13A>G
ENST00000402066.5:c.1303-13A>G	ENSP00000384497.1:n.1303-13A>G
NM_001304522.1:c.640-13A>G	NP_001291451.1:n.640-13A>G
NM_001308259.1:c.832-13A>G	NP_001295188.1:n.832-13A>G
NM_003382.4:c.880-13A>G	NP_003373.2:n.880-13A>G
NR_130758.1:n.1066-13A>G
XM_005249561.2:c.955-13A>G	XP_005249618.1:n.955-13A>G
XM_006716107.1:c.880-13A>G	XP_006716170.1:n.880-13A>G
XM_006716108.2:c.691-13A>G	XP_006716171.1:n.691-13A>G
XM_011516550.1:c.832-13A>G	XP_011514852.1:n.832-13A>G
XM_011516552.1:c.466-13A>G	XP_011514854.1:n.466-13A>G
XM_005249561.3:c.955-13A>G	XP_005249618.1:n.955-13A>G
XM_006716107.2:c.880-13A>G	XP_006716170.1:n.880-13A>G
XM_006716108.3:c.691-13A>G	XP_006716171.1:n.691-13A>G
XM_011516550.2:c.832-13A>G	XP_011514852.1:n.832-13A>G
XM_017012580.1:c.466-13A>G	XP_016868069.1:n.466-13A>G
XM_024446914.1:c.955-13A>G	XP_024302682.1:n.955-13A>G
XM_024446915.1:c.955-13A>G	XP_024302683.1:n.955-13A>G
XM_024446916.1:c.880-13A>G	XP_024302684.1:n.880-13A>G
XM_024446917.1:c.691-13A>G	XP_024302685.1:n.691-13A>G
XM_024446918.1:c.466-13A>G	XP_024302686.1:n.466-13A>G
NM_003382.5:c.880-13A>G MANE Select	NP_003373.2:n.880-13A>G
NM_001304522.2:c.640-13A>G	NP_001291451.1:n.640-13A>G
NR_130758.2:n.976-13A>G