Canonical Allele Identifier: CA369941523
Gene: VIPR2 HGNC NCBI

Linked Data

dbSNP Id: rs2071624

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.159034635G>T , CM000669.2:g.159034635G>T GRCh38
NC_000007.13:g.158827326G>T , CM000669.1:g.158827326G>T GRCh37
NC_000007.12:g.158520087G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000262178.7:c.825C>A MANE Select ENSP00000262178.2:p.Asn275Lys
ENST00000262178.6:c.825C>A ENSP00000262178.2:p.Asn275Lys
ENST00000377633.7:c.777C>A ENSP00000366860.3:p.Asn259Lys
ENST00000402066.5:c.1248C>A ENSP00000384497.1:p.Asn416Lys
NM_001304522.1:c.585C>A NP_001291451.1:p.Asn195Lys
NM_001308259.1:c.777C>A NP_001295188.1:p.Asn259Lys
NM_003382.4:c.825C>A NP_003373.2:p.Asn275Lys
NR_130758.1:n.1011C>A
XM_005249561.2:c.900C>A XP_005249618.1:p.Asn300Lys
XM_006716107.1:c.825C>A XP_006716170.1:p.Asn275Lys
XM_006716108.2:c.636C>A XP_006716171.1:p.Asn212Lys
XM_011516550.1:c.777C>A XP_011514852.1:p.Asn259Lys
XM_011516552.1:c.411C>A XP_011514854.1:p.Asn137Lys
XR_242047.2:n.1220C>A
XM_005249561.3:c.900C>A XP_005249618.1:p.Asn300Lys
XM_006716107.2:c.825C>A XP_006716170.1:p.Asn275Lys
XM_006716108.3:c.636C>A XP_006716171.1:p.Asn212Lys
XM_011516550.2:c.777C>A XP_011514852.1:p.Asn259Lys
XM_017012580.1:c.411C>A XP_016868069.1:p.Asn137Lys
XM_024446914.1:c.900C>A XP_024302682.1:p.Asn300Lys
XM_024446915.1:c.900C>A XP_024302683.1:p.Asn300Lys
XM_024446916.1:c.825C>A XP_024302684.1:p.Asn275Lys
XM_024446917.1:c.636C>A XP_024302685.1:p.Asn212Lys
XM_024446918.1:c.411C>A XP_024302686.1:p.Asn137Lys
NM_003382.5:c.825C>A MANE Select NP_003373.2:p.Asn275Lys
NM_001304522.2:c.585C>A NP_001291451.1:p.Asn195Lys
NR_130758.2:n.921C>A