Canonical Allele Identifier: CA369941169

Gene: VIPR2

Linked Data

• MyVariant Identifiers: chr7:g.158827288A>C (hg19) ; chr7:g.159034597A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.159034597A>C , CM000669.2:g.159034597A>C	GRCh38
NC_000007.13:g.158827288A>C , CM000669.1:g.158827288A>C	GRCh37
NC_000007.12:g.158520049A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262178.7:c.863T>G MANE Select	ENSP00000262178.2:p.Ile288Ser
ENST00000262178.6:c.863T>G	ENSP00000262178.2:p.Ile288Ser
ENST00000377633.7:c.815T>G	ENSP00000366860.3:p.Ile272Ser
ENST00000402066.5:c.1286T>G	ENSP00000384497.1:p.Ile429Ser
NM_001304522.1:c.623T>G	NP_001291451.1:p.Ile208Ser
NM_001308259.1:c.815T>G	NP_001295188.1:p.Ile272Ser
NM_003382.4:c.863T>G	NP_003373.2:p.Ile288Ser
NR_130758.1:n.1049T>G
XM_005249561.2:c.938T>G	XP_005249618.1:p.Ile313Ser
XM_006716107.1:c.863T>G	XP_006716170.1:p.Ile288Ser
XM_006716108.2:c.674T>G	XP_006716171.1:p.Ile225Ser
XM_011516550.1:c.815T>G	XP_011514852.1:p.Ile272Ser
XM_011516552.1:c.449T>G	XP_011514854.1:p.Ile150Ser
XR_242047.2:n.1258T>G
XM_005249561.3:c.938T>G	XP_005249618.1:p.Ile313Ser
XM_006716107.2:c.863T>G	XP_006716170.1:p.Ile288Ser
XM_006716108.3:c.674T>G	XP_006716171.1:p.Ile225Ser
XM_011516550.2:c.815T>G	XP_011514852.1:p.Ile272Ser
XM_017012580.1:c.449T>G	XP_016868069.1:p.Ile150Ser
XM_024446914.1:c.938T>G	XP_024302682.1:p.Ile313Ser
XM_024446915.1:c.938T>G	XP_024302683.1:p.Ile313Ser
XM_024446916.1:c.863T>G	XP_024302684.1:p.Ile288Ser
XM_024446917.1:c.674T>G	XP_024302685.1:p.Ile225Ser
XM_024446918.1:c.449T>G	XP_024302686.1:p.Ile150Ser
NM_003382.5:c.863T>G MANE Select	NP_003373.2:p.Ile288Ser
NM_001304522.2:c.623T>G	NP_001291451.1:p.Ile208Ser
NR_130758.2:n.959T>G