Canonical Allele Identifier: CA459004889

Gene: VIPR2

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159029367T>G , CM000669.2:g.159029367T>G	GRCh38
NC_000007.13:g.158822058T>G , CM000669.1:g.158822058T>G	GRCh37
NC_000007.12:g.158514819T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.*1249A>C MANE Select	ENSP00000262178.2:n.*1249A>C
ENST00000262178.6:c.*1249A>C	ENSP00000262178.2:n.*1249A>C
NM_001304522.1:c.*1249A>C	NP_001291451.1:n.*1249A>C
NM_001308259.1:c.*1249A>C	NP_001295188.1:n.*1249A>C
NM_003382.4:c.*1249A>C	NP_003373.2:n.*1249A>C
NR_130758.1:n.3086A>C
XM_005249561.3:c.*1249A>C	XP_005249618.1:n.*1249A>C
XM_017012580.1:c.*1249A>C	XP_016868069.1:n.*1249A>C
XM_024446914.1:c.*1249A>C	XP_024302682.1:n.*1249A>C
XM_024446915.1:c.*1249A>C	XP_024302683.1:n.*1249A>C
XM_024446916.1:c.*1249A>C	XP_024302684.1:n.*1249A>C
XM_024446917.1:c.*1249A>C	XP_024302685.1:n.*1249A>C
XM_024446918.1:c.*1249A>C	XP_024302686.1:n.*1249A>C
NM_003382.5:c.*1249A>C MANE Select	NP_003373.2:n.*1249A>C
NM_001304522.2:c.*1249A>C	NP_001291451.1:n.*1249A>C
NR_130758.2:n.2996A>C