Canonical Allele Identifier: CA489741215

Gene: IVD

Linked Data

• MyVariant Identifiers: chr15:g.40703857T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40411658T>G , CM000677.2:g.40411658T>G	GRCh38
NC_000015.9:g.40703857T>G , CM000677.1:g.40703857T>G	GRCh37
NC_000015.8:g.38491149T>G	NCBI36
NG_011986.1:g.11172T>G
NG_011986.2:g.11174T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479013.7:c.564T>G	ENSP00000417990.3:p.Ala188=
ENST00000487418.8:c.654T>G MANE Select	ENSP00000418397.3:p.Ala218=
ENST00000650656.1:c.573T>G	ENSP00000498731.1:p.Ala191=
ENST00000651168.1:c.663T>G	ENSP00000499074.1:p.Ala221=
ENST00000473112.6:c.413T>G
ENST00000479013.6:c.573T>G	ENSP00000417990.2:p.Ala191=
ENST00000481262.6:c.260T>G
ENST00000484250.1:n.277T>G
ENST00000487418.6:c.663T>G	ENSP00000418397.2:p.Ala221=
ENST00000491554.6:c.51T>G	ENSP00000453146.1:p.Ala17=
ENST00000558610.5:c.606T>G	ENSP00000453821.1:p.Ala202=
NM_001159508.1:c.573T>G	NP_001152980.1:p.Ala191=
NM_002225.3:c.663T>G	NP_002216.2:p.Ala221=
XM_005254350.2:c.663T>G	XP_005254407.1:p.Ala221=
XM_005254356.2:c.663T>G	XP_005254413.1:p.Ala221=
XM_006720491.2:c.606T>G	XP_006720554.1:p.Ala202=
XM_006720492.2:c.663T>G	XP_006720555.1:p.Ala221=
XM_006720493.2:c.663T>G	XP_006720556.1:p.Ala221=
XM_006720494.2:c.663T>G	XP_006720557.1:p.Ala221=
XM_006720495.2:c.663T>G	XP_006720558.1:p.Ala221=
XM_011521523.1:c.663T>G	XP_011519825.1:p.Ala221=
XM_011521524.1:c.663T>G	XP_011519826.1:p.Ala221=
XR_243097.3:n.663T>G
XR_243098.2:n.663T>G
XR_429453.2:n.764T>G
NM_001159508.2:c.564T>G	NP_001152980.2:p.Ala188=
NM_001354597.2:c.606T>G	NP_001341526.1:p.Ala202=
NM_001354598.2:c.654T>G	NP_001341527.2:p.Ala218=
NM_001354599.2:c.741T>G	NP_001341528.2:p.Ala247=
NM_001354600.2:c.741T>G	NP_001341529.2:p.Ala247=
NM_001354601.2:c.654T>G	NP_001341530.2:p.Ala218=
NM_002225.4:c.654T>G	NP_002216.3:p.Ala218=
NR_148925.1:n.1064T>G
XM_006720495.3:c.663T>G	XP_006720558.1:p.Ala221=
XM_017022149.1:c.750T>G	XP_016877638.1:p.Ala250=
XM_017022150.1:c.750T>G	XP_016877639.1:p.Ala250=
XM_017022153.1:c.750T>G	XP_016877642.1:p.Ala250=
XM_017022154.2:c.693T>G	XP_016877643.1:p.Ala231=
XM_017022155.2:c.750T>G	XP_016877644.1:p.Ala250=
XM_017022157.1:c.750T>G	XP_016877646.1:p.Ala250=
XM_017022158.2:c.750T>G	XP_016877647.1:p.Ala250=
XR_001751263.1:n.1013T>G
XR_001751264.1:n.1054T>G
NM_001159508.3:c.564T>G	NP_001152980.2:p.Ala188=
NM_001354597.3:c.606T>G	NP_001341526.1:p.Ala202=
NM_001354598.3:c.654T>G	NP_001341527.2:p.Ala218=
NM_001354599.3:c.741T>G	NP_001341528.2:p.Ala247=
NM_001354600.3:c.741T>G	NP_001341529.2:p.Ala247=
NM_001354601.3:c.654T>G	NP_001341530.2:p.Ala218=
NM_002225.5:c.654T>G MANE Select	NP_002216.3:p.Ala218=
NR_148925.2:n.1066T>G