Canonical Allele Identifier: CA12309247

Gene: IPCEF1 OPRM1 CNKSR3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.154166286C>T , CM000668.2:g.154166286C>T	GRCh38
NC_000006.11:g.154487421C>T , CM000668.1:g.154487421C>T	GRCh37
NC_000006.10:g.154529113C>T	NCBI36
NG_021208.1:g.160786C>T
NG_021208.2:g.160786C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367220.9:c.1104+1634G>A (IPCEF1) MANE Select	ENSP00000356189.4:n.1104+1634G>A
ENST00000673182.1:c.2487+1634G>A	ENSP00000499846.1:n.2487+1634G>A
ENST00000265198.8:c.1101+1634G>A (IPCEF1)	ENSP00000265198.4:n.1101+1634G>A
ENST00000337049.8:c.1164+74814C>T (OPRM1)	ENSP00000338381.4:n.1164+74814C>T
ENST00000367220.8:c.1104+1634G>A (IPCEF1)	ENSP00000356189.4:n.1104+1634G>A
ENST00000422970.6:c.1104+1634G>A (IPCEF1)	ENSP00000394751.2:n.1104+1634G>A
ENST00000519344.5:c.1017+1634G>A (IPCEF1)	ENSP00000430287.1:n.1017+1634G>A
ENST00000522590.1:n.1128+1634G>A (IPCEF1)
ENST00000524150.2:c.*250+74814C>T (OPRM1)	ENSP00000430575.1:n.*250+74814C>T
ENST00000616478.4:c.2487+1634G>A (CNKSR3)	ENSP00000478800.1:n.2487+1634G>A
NM_001008503.2:c.1164+74814C>T (OPRM1)	NP_001008503.2:n.1164+74814C>T
NM_001130699.1:c.1104+1634G>A (IPCEF1)	NP_001124171.1:n.1104+1634G>A
NM_001130700.1:c.1104+1634G>A (IPCEF1)	NP_001124172.1:n.1104+1634G>A
NM_015553.2:c.1101+1634G>A (IPCEF1)	NP_056368.1:n.1101+1634G>A
XM_005266919.3:c.1104+1634G>A (IPCEF1)	XP_005266976.1:n.1104+1634G>A
XM_005266920.3:c.1104+1634G>A (IPCEF1)	XP_005266977.1:n.1104+1634G>A
XM_005266921.3:c.1104+1634G>A (IPCEF1)	XP_005266978.1:n.1104+1634G>A
XM_005266922.3:c.1104+1634G>A (IPCEF1)	XP_005266979.1:n.1104+1634G>A
XM_005266923.2:c.1101+1634G>A (IPCEF1)	XP_005266980.1:n.1101+1634G>A
XM_011535739.1:c.1104+1634G>A (IPCEF1)	XP_011534041.1:n.1104+1634G>A
XM_011535740.1:c.1104+1634G>A (IPCEF1)	XP_011534042.1:n.1104+1634G>A
XM_011535741.1:c.1104+1634G>A (IPCEF1)	XP_011534043.1:n.1104+1634G>A
XM_011535742.1:c.1101+1634G>A (IPCEF1)	XP_011534044.1:n.1101+1634G>A
XM_011535744.1:c.720+1634G>A (IPCEF1)	XP_011534046.1:n.720+1634G>A
NM_001008503.3:c.1164+74814C>T (OPRM1)	NP_001008503.2:n.1164+74814C>T
NM_001130699.2:c.1104+1634G>A (IPCEF1)	NP_001124171.1:n.1104+1634G>A
NM_001130700.2:c.1104+1634G>A (IPCEF1) MANE Select	NP_001124172.1:n.1104+1634G>A
NM_015553.3:c.1101+1634G>A (IPCEF1)	NP_056368.1:n.1101+1634G>A
NM_001394799.1:c.1104+1634G>A (IPCEF1)	NP_001381728.1:n.1104+1634G>A
NM_001394800.1:c.1104+1634G>A (IPCEF1)	NP_001381729.1:n.1104+1634G>A
NM_001394801.1:c.1104+1634G>A (IPCEF1)	NP_001381730.1:n.1104+1634G>A
NM_001394802.1:c.1101+1634G>A (IPCEF1)	NP_001381731.1:n.1101+1634G>A