Canonical Allele Identifier: CA12552815

Gene: VIPR2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159028278C>T , CM000669.2:g.159028278C>T	GRCh38
NC_000007.13:g.158820969C>T , CM000669.1:g.158820969C>T	GRCh37
NC_000007.12:g.158513730C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.*2338G>A MANE Select	ENSP00000262178.2:n.*2338G>A
ENST00000262178.6:c.*2338G>A	ENSP00000262178.2:n.*2338G>A
NM_001304522.1:c.*2338G>A	NP_001291451.1:n.*2338G>A
NM_001308259.1:c.*2338G>A	NP_001295188.1:n.*2338G>A
NM_003382.4:c.*2338G>A	NP_003373.2:n.*2338G>A
NR_130758.1:n.4175G>A
XM_005249561.3:c.*2338G>A	XP_005249618.1:n.*2338G>A
XM_017012580.1:c.*2338G>A	XP_016868069.1:n.*2338G>A
XM_024446914.1:c.*2338G>A	XP_024302682.1:n.*2338G>A
XM_024446915.1:c.*2338G>A	XP_024302683.1:n.*2338G>A
XM_024446916.1:c.*2338G>A	XP_024302684.1:n.*2338G>A
XM_024446917.1:c.*2338G>A	XP_024302685.1:n.*2338G>A
XM_024446918.1:c.*2338G>A	XP_024302686.1:n.*2338G>A
NM_003382.5:c.*2338G>A MANE Select	NP_003373.2:n.*2338G>A
NM_001304522.2:c.*2338G>A	NP_001291451.1:n.*2338G>A
NR_130758.2:n.4085G>A