Canonical Allele Identifier: CA459008432

Gene: VIPR2

Linked Data

• MyVariant Identifiers: chr7:g.158827338G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159034647G>A , CM000669.2:g.159034647G>A	GRCh38
NC_000007.13:g.158827338G>A , CM000669.1:g.158827338G>A	GRCh37
NC_000007.12:g.158520099G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.813C>T MANE Select	ENSP00000262178.2:p.Cys271=
ENST00000262178.6:c.813C>T	ENSP00000262178.2:p.Cys271=
ENST00000377633.7:c.765C>T	ENSP00000366860.3:p.Cys255=
ENST00000402066.5:c.1236C>T	ENSP00000384497.1:p.Cys412=
NM_001304522.1:c.573C>T	NP_001291451.1:p.Cys191=
NM_001308259.1:c.765C>T	NP_001295188.1:p.Cys255=
NM_003382.4:c.813C>T	NP_003373.2:p.Cys271=
NR_130758.1:n.999C>T
XM_005249561.2:c.888C>T	XP_005249618.1:p.Cys296=
XM_006716107.1:c.813C>T	XP_006716170.1:p.Cys271=
XM_006716108.2:c.624C>T	XP_006716171.1:p.Cys208=
XM_011516550.1:c.765C>T	XP_011514852.1:p.Cys255=
XM_011516552.1:c.399C>T	XP_011514854.1:p.Cys133=
XR_242047.2:n.1208C>T
XM_005249561.3:c.888C>T	XP_005249618.1:p.Cys296=
XM_006716107.2:c.813C>T	XP_006716170.1:p.Cys271=
XM_006716108.3:c.624C>T	XP_006716171.1:p.Cys208=
XM_011516550.2:c.765C>T	XP_011514852.1:p.Cys255=
XM_017012580.1:c.399C>T	XP_016868069.1:p.Cys133=
XM_024446914.1:c.888C>T	XP_024302682.1:p.Cys296=
XM_024446915.1:c.888C>T	XP_024302683.1:p.Cys296=
XM_024446916.1:c.813C>T	XP_024302684.1:p.Cys271=
XM_024446917.1:c.624C>T	XP_024302685.1:p.Cys208=
XM_024446918.1:c.399C>T	XP_024302686.1:p.Cys133=
NM_003382.5:c.813C>T MANE Select	NP_003373.2:p.Cys271=
NM_001304522.2:c.573C>T	NP_001291451.1:p.Cys191=
NR_130758.2:n.909C>T