Canonical Allele Identifier: CA1360385108

Gene: VIPR1

Genomic Alleles

HGVS	Genome Assembly
NC_000003.12:g.42526948C= , CM000665.2:g.42526948C=	GRCh38
NC_000003.11:g.42568440C= , CM000665.1:g.42568440C=	GRCh37
NC_000003.10:g.42543444C=	NCBI36
NG_030371.1:g.42650C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000325123.5:c.400-445C= MANE Select	ENSP00000327246.4:n.400-445C=
ENST00000325123.4:c.400-445C=	ENSP00000327246.4:n.400-445C=
ENST00000433647.5:c.277-445C=	ENSP00000394950.1:n.277-445C=
ENST00000436487.5:c.*156-448C=	ENSP00000393215.1:n.*156-448C=
ENST00000438259.6:c.26+955C=	ENSP00000415371.2:n.26+955C=
ENST00000439731.5:c.400-445C=	ENSP00000403478.1:n.400-445C=
ENST00000439910.5:c.*155+955C=	ENSP00000403680.1:n.*155+955C=
ENST00000443646.5:c.*156-445C=	ENSP00000388479.1:n.*156-445C=
ENST00000446673.5:c.*156-445C=	ENSP00000396204.1:n.*156-445C=
ENST00000450274.5:c.277-445C=	ENSP00000415013.1:n.277-445C=
ENST00000473575.1:n.272-445C=
ENST00000543411.5:c.259-448C=	ENSP00000445701.1:n.259-448C=
NM_001251882.1:c.277-445C=	NP_001238811.1:n.277-445C=
NM_001251883.1:c.26+955C=	NP_001238812.1:n.26+955C=
NM_001251884.1:c.259-448C=	NP_001238813.1:n.259-448C=
NM_001251885.1:c.319-445C=	NP_001238814.1:n.319-445C=
NM_004624.3:c.400-445C=	NP_004615.2:n.400-445C=
XM_005265437.2:c.400-448C=	XP_005265494.1:n.400-448C=
XM_005265438.3:c.277-445C=	XP_005265495.1:n.277-445C=
XM_005265439.2:c.259-445C=	XP_005265496.1:n.259-445C=
XM_011534079.1:c.277-445C=	XP_011532381.1:n.277-445C=
XM_011534080.1:c.400-445C=	XP_011532382.1:n.400-445C=
XR_940499.1:n.507-445C=
XR_940500.1:n.507-445C=
XM_011534080.2:c.400-445C=	XP_011532382.1:n.400-445C=
XR_001740254.1:n.507-445C=
XR_001740255.1:n.1053-445C=
XR_940500.2:n.507-445C=
NM_004624.4:c.400-445C= MANE Select	NP_004615.2:n.400-445C=
NM_001251882.2:c.277-445C=	NP_001238811.1:n.277-445C=
NM_001251883.2:c.26+955C=	NP_001238812.1:n.26+955C=
NM_001251884.2:c.259-448C=	NP_001238813.1:n.259-448C=
NM_001251885.2:c.319-445C=	NP_001238814.1:n.319-445C=