Canonical Allele Identifier: CA2171765974

Gene: IVD

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40411663G= , CM000677.2:g.40411663G=	GRCh38
NC_000015.9:g.40703862G= , CM000677.1:g.40703862G=	GRCh37
NC_000015.8:g.38491154G=	NCBI36
NG_011986.1:g.11177G=
NG_011986.2:g.11179G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479013.7:c.569G=	ENSP00000417990.3:p.Arg190=
ENST00000487418.8:c.659G= MANE Select	ENSP00000418397.3:p.Arg220=
ENST00000650656.1:c.578G=	ENSP00000498731.1:p.Arg193=
ENST00000651168.1:c.668G=	ENSP00000499074.1:p.Arg223=
ENST00000473112.6:c.418G=
ENST00000479013.6:c.578G=	ENSP00000417990.2:p.Arg193=
ENST00000481262.6:c.265G=
ENST00000484250.1:n.282G=
ENST00000487418.6:c.668G=	ENSP00000418397.2:p.Arg223=
ENST00000491554.6:c.56G=	ENSP00000453146.1:p.Arg19=
ENST00000558610.5:c.611G=	ENSP00000453821.1:p.Arg204=
NM_001159508.1:c.578G=	NP_001152980.1:p.Arg193=
NM_002225.3:c.668G=	NP_002216.2:p.Arg223=
XM_005254350.2:c.668G=	XP_005254407.1:p.Arg223=
XM_005254356.2:c.668G=	XP_005254413.1:p.Arg223=
XM_006720491.2:c.611G=	XP_006720554.1:p.Arg204=
XM_006720492.2:c.668G=	XP_006720555.1:p.Arg223=
XM_006720493.2:c.668G=	XP_006720556.1:p.Arg223=
XM_006720494.2:c.668G=	XP_006720557.1:p.Arg223=
XM_006720495.2:c.668G=	XP_006720558.1:p.Arg223=
XM_011521523.1:c.668G=	XP_011519825.1:p.Arg223=
XM_011521524.1:c.668G=	XP_011519826.1:p.Arg223=
XR_243097.3:n.668G=
XR_243098.2:n.668G=
XR_429453.2:n.769G=
NM_001159508.2:c.569G=	NP_001152980.2:p.Arg190=
NM_001354597.2:c.611G=	NP_001341526.1:p.Arg204=
NM_001354598.2:c.659G=	NP_001341527.2:p.Arg220=
NM_001354599.2:c.746G=	NP_001341528.2:p.Arg249=
NM_001354600.2:c.746G=	NP_001341529.2:p.Arg249=
NM_001354601.2:c.659G=	NP_001341530.2:p.Arg220=
NM_002225.4:c.659G=	NP_002216.3:p.Arg220=
NR_148925.1:n.1069G=
XM_006720495.3:c.668G=	XP_006720558.1:p.Arg223=
XM_017022149.1:c.755G=	XP_016877638.1:p.Arg252=
XM_017022150.1:c.755G=	XP_016877639.1:p.Arg252=
XM_017022153.1:c.755G=	XP_016877642.1:p.Arg252=
XM_017022154.2:c.698G=	XP_016877643.1:p.Arg233=
XM_017022155.2:c.755G=	XP_016877644.1:p.Arg252=
XM_017022157.1:c.755G=	XP_016877646.1:p.Arg252=
XM_017022158.2:c.755G=	XP_016877647.1:p.Arg252=
XR_001751263.1:n.1018G=
XR_001751264.1:n.1059G=
NM_001159508.3:c.569G=	NP_001152980.2:p.Arg190=
NM_001354597.3:c.611G=	NP_001341526.1:p.Arg204=
NM_001354598.3:c.659G=	NP_001341527.2:p.Arg220=
NM_001354599.3:c.746G=	NP_001341528.2:p.Arg249=
NM_001354600.3:c.746G=	NP_001341529.2:p.Arg249=
NM_001354601.3:c.659G=	NP_001341530.2:p.Arg220=
NM_002225.5:c.659G= MANE Select	NP_002216.3:p.Arg220=
NR_148925.2:n.1071G=