Canonical Allele Identifier: CA12668861

Gene: VIPR2

Linked Data - Predicted Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159054238G>T , CM000669.2:g.159054238G>T	GRCh38
NC_000007.13:g.158846929G>T , CM000669.1:g.158846929G>T	GRCh37
NC_000007.12:g.158539690G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.455+4243C>A MANE Select	ENSP00000262178.2:n.455+4243C>A
ENST00000262178.6:c.455+4243C>A	ENSP00000262178.2:n.455+4243C>A
ENST00000377633.7:c.407+4243C>A	ENSP00000366860.3:n.407+4243C>A
ENST00000402066.5:c.878+4243C>A	ENSP00000384497.1:n.878+4243C>A
NM_001304522.1:c.358-17336C>A	NP_001291451.1:n.358-17336C>A
NM_001308259.1:c.407+4243C>A	NP_001295188.1:n.407+4243C>A
NM_003382.4:c.455+4243C>A	NP_003373.2:n.455+4243C>A
NR_130758.1:n.641+4243C>A
XM_005249561.2:c.530+4243C>A	XP_005249618.1:n.530+4243C>A
XM_006716107.1:c.455+4243C>A	XP_006716170.1:n.455+4243C>A
XM_006716108.2:c.266+4243C>A	XP_006716171.1:n.266+4243C>A
XM_011516550.1:c.407+4243C>A	XP_011514852.1:n.407+4243C>A
XM_011516552.1:c.41+4243C>A	XP_011514854.1:n.41+4243C>A
XR_242047.2:n.641+4243C>A
XM_005249561.3:c.530+4243C>A	XP_005249618.1:n.530+4243C>A
XM_006716107.2:c.455+4243C>A	XP_006716170.1:n.455+4243C>A
XM_006716108.3:c.266+4243C>A	XP_006716171.1:n.266+4243C>A
XM_011516550.2:c.407+4243C>A	XP_011514852.1:n.407+4243C>A
XM_017012580.1:c.41+4243C>A	XP_016868069.1:n.41+4243C>A
XM_024446914.1:c.530+4243C>A	XP_024302682.1:n.530+4243C>A
XM_024446915.1:c.530+4243C>A	XP_024302683.1:n.530+4243C>A
XM_024446916.1:c.455+4243C>A	XP_024302684.1:n.455+4243C>A
XM_024446917.1:c.266+4243C>A	XP_024302685.1:n.266+4243C>A
XM_024446918.1:c.41+4243C>A	XP_024302686.1:n.41+4243C>A
NM_003382.5:c.455+4243C>A MANE Select	NP_003373.2:n.455+4243C>A
NM_001304522.2:c.358-17336C>A	NP_001291451.1:n.358-17336C>A
NR_130758.2:n.551+4243C>A