Canonical Allele Identifier: CA489759018

Gene: IVD

Linked Data

• MyVariant Identifiers: chr15:g.40700161C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40407962C>T , CM000677.2:g.40407962C>T	GRCh38
NC_000015.9:g.40700161C>T , CM000677.1:g.40700161C>T	GRCh37
NC_000015.8:g.38487453C>T	NCBI36
NG_011986.1:g.7476C>T
NG_011986.2:g.7478C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479013.7:c.168C>T	ENSP00000417990.3:p.Asn56=
ENST00000487418.8:c.258C>T MANE Select	ENSP00000418397.3:p.Asn86=
ENST00000610693.5:c.345C>T	ENSP00000479359.2:p.Asn115=
ENST00000650656.1:c.177C>T	ENSP00000498731.1:p.Asn59=
ENST00000651168.1:c.267C>T	ENSP00000499074.1:p.Asn89=
ENST00000473112.6:c.17C>T
ENST00000479013.6:c.177C>T	ENSP00000417990.2:p.Asn59=
ENST00000487418.6:c.267C>T	ENSP00000418397.2:p.Asn89=
ENST00000558610.5:c.210C>T	ENSP00000453821.1:p.Asn70=
ENST00000610693.4:c.354C>T	ENSP00000479359.1:p.Asn118=
NM_001159508.1:c.177C>T	NP_001152980.1:p.Asn59=
NM_002225.3:c.267C>T	NP_002216.2:p.Asn89=
XM_005254350.2:c.267C>T	XP_005254407.1:p.Asn89=
XM_005254356.2:c.267C>T	XP_005254413.1:p.Asn89=
XM_006720491.2:c.210C>T	XP_006720554.1:p.Asn70=
XM_006720492.2:c.267C>T	XP_006720555.1:p.Asn89=
XM_006720493.2:c.267C>T	XP_006720556.1:p.Asn89=
XM_006720494.2:c.267C>T	XP_006720557.1:p.Asn89=
XM_006720495.2:c.267C>T	XP_006720558.1:p.Asn89=
XM_011521523.1:c.267C>T	XP_011519825.1:p.Asn89=
XM_011521524.1:c.267C>T	XP_011519826.1:p.Asn89=
XR_243097.3:n.267C>T
XR_243098.2:n.267C>T
XR_429453.2:n.368C>T
NM_001159508.2:c.168C>T	NP_001152980.2:p.Asn56=
NM_001354597.2:c.210C>T	NP_001341526.1:p.Asn70=
NM_001354598.2:c.258C>T	NP_001341527.2:p.Asn86=
NM_001354599.2:c.345C>T	NP_001341528.2:p.Asn115=
NM_001354600.2:c.345C>T	NP_001341529.2:p.Asn115=
NM_001354601.2:c.258C>T	NP_001341530.2:p.Asn86=
NM_002225.4:c.258C>T	NP_002216.3:p.Asn86=
NR_148925.1:n.668C>T
XM_006720495.3:c.267C>T	XP_006720558.1:p.Asn89=
XM_017022149.1:c.354C>T	XP_016877638.1:p.Asn118=
XM_017022150.1:c.354C>T	XP_016877639.1:p.Asn118=
XM_017022153.1:c.354C>T	XP_016877642.1:p.Asn118=
XM_017022154.2:c.297C>T	XP_016877643.1:p.Asn99=
XM_017022155.2:c.354C>T	XP_016877644.1:p.Asn118=
XM_017022157.1:c.354C>T	XP_016877646.1:p.Asn118=
XM_017022158.2:c.354C>T	XP_016877647.1:p.Asn118=
XR_001751263.1:n.617C>T
XR_001751264.1:n.658C>T
NM_001159508.3:c.168C>T	NP_001152980.2:p.Asn56=
NM_001354597.3:c.210C>T	NP_001341526.1:p.Asn70=
NM_001354598.3:c.258C>T	NP_001341527.2:p.Asn86=
NM_001354599.3:c.345C>T	NP_001341528.2:p.Asn115=
NM_001354600.3:c.345C>T	NP_001341529.2:p.Asn115=
NM_001354601.3:c.258C>T	NP_001341530.2:p.Asn86=
NM_002225.5:c.258C>T MANE Select	NP_002216.3:p.Asn86=
NR_148925.2:n.670C>T