Canonical Allele Identifier: CA391717497

Gene: IVD

Linked Data

• gnomAD v4: 15-40411576-G-A
• MyVariant Identifiers: chr15:g.40703775G>A (hg19) ; chr15:g.40411576G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40411576G>A , CM000677.2:g.40411576G>A	GRCh38
NC_000015.9:g.40703775G>A , CM000677.1:g.40703775G>A	GRCh37
NC_000015.8:g.38491067G>A	NCBI36
NG_011986.1:g.11090G>A
NG_011986.2:g.11092G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479013.7:c.482G>A	ENSP00000417990.3:p.Gly161Asp
ENST00000487418.8:c.572G>A MANE Select	ENSP00000418397.3:p.Gly191Asp
ENST00000650656.1:c.491G>A	ENSP00000498731.1:p.Gly164Asp
ENST00000651168.1:c.581G>A	ENSP00000499074.1:p.Gly194Asp
ENST00000473112.6:c.331G>A
ENST00000479013.6:c.491G>A	ENSP00000417990.2:p.Gly164Asp
ENST00000481262.6:c.178G>A
ENST00000484250.1:n.195G>A
ENST00000487418.6:c.581G>A	ENSP00000418397.2:p.Gly194Asp
ENST00000558610.5:c.524G>A	ENSP00000453821.1:p.Gly175Asp
NM_001159508.1:c.491G>A	NP_001152980.1:p.Gly164Asp
NM_002225.3:c.581G>A	NP_002216.2:p.Gly194Asp
XM_005254350.2:c.581G>A	XP_005254407.1:p.Gly194Asp
XM_005254356.2:c.581G>A	XP_005254413.1:p.Gly194Asp
XM_006720491.2:c.524G>A	XP_006720554.1:p.Gly175Asp
XM_006720492.2:c.581G>A	XP_006720555.1:p.Gly194Asp
XM_006720493.2:c.581G>A	XP_006720556.1:p.Gly194Asp
XM_006720494.2:c.581G>A	XP_006720557.1:p.Gly194Asp
XM_006720495.2:c.581G>A	XP_006720558.1:p.Gly194Asp
XM_011521523.1:c.581G>A	XP_011519825.1:p.Gly194Asp
XM_011521524.1:c.581G>A	XP_011519826.1:p.Gly194Asp
XR_243097.3:n.581G>A
XR_243098.2:n.581G>A
XR_429453.2:n.682G>A
NM_001159508.2:c.482G>A	NP_001152980.2:p.Gly161Asp
NM_001354597.2:c.524G>A	NP_001341526.1:p.Gly175Asp
NM_001354598.2:c.572G>A	NP_001341527.2:p.Gly191Asp
NM_001354599.2:c.659G>A	NP_001341528.2:p.Gly220Asp
NM_001354600.2:c.659G>A	NP_001341529.2:p.Gly220Asp
NM_001354601.2:c.572G>A	NP_001341530.2:p.Gly191Asp
NM_002225.4:c.572G>A	NP_002216.3:p.Gly191Asp
NR_148925.1:n.982G>A
XM_006720495.3:c.581G>A	XP_006720558.1:p.Gly194Asp
XM_017022149.1:c.668G>A	XP_016877638.1:p.Gly223Asp
XM_017022150.1:c.668G>A	XP_016877639.1:p.Gly223Asp
XM_017022153.1:c.668G>A	XP_016877642.1:p.Gly223Asp
XM_017022154.2:c.611G>A	XP_016877643.1:p.Gly204Asp
XM_017022155.2:c.668G>A	XP_016877644.1:p.Gly223Asp
XM_017022157.1:c.668G>A	XP_016877646.1:p.Gly223Asp
XM_017022158.2:c.668G>A	XP_016877647.1:p.Gly223Asp
XR_001751263.1:n.931G>A
XR_001751264.1:n.972G>A
NM_001159508.3:c.482G>A	NP_001152980.2:p.Gly161Asp
NM_001354597.3:c.524G>A	NP_001341526.1:p.Gly175Asp
NM_001354598.3:c.572G>A	NP_001341527.2:p.Gly191Asp
NM_001354599.3:c.659G>A	NP_001341528.2:p.Gly220Asp
NM_001354600.3:c.659G>A	NP_001341529.2:p.Gly220Asp
NM_001354601.3:c.572G>A	NP_001341530.2:p.Gly191Asp
NM_002225.5:c.572G>A MANE Select	NP_002216.3:p.Gly191Asp
NR_148925.2:n.984G>A