Canonical Allele Identifier: CA221929

Gene: IVD

Linked Data

• ClinVar Variation Id: 94050
• ClinVar RCV Id: RCV000417380 ; RCV000557255
• dbSNP Id: rs398123679
• MyVariant Identifiers: chr15:g.40708489G>A (hg19) ; chr15:g.40416290G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40416290G>A , CM000677.2:g.40416290G>A	GRCh38
NC_000015.9:g.40708489G>A , CM000677.1:g.40708489G>A	GRCh37
NC_000015.8:g.38495781G>A	NCBI36
NG_011986.1:g.15804G>A
NG_011986.2:g.15806G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479013.7:c.976G>A	ENSP00000417990.3:p.Asp326Asn
ENST00000487418.8:c.1066G>A MANE Select	ENSP00000418397.3:p.Asp356Asn
ENST00000650656.1:c.985G>A	ENSP00000498731.1:p.Asp329Asn
ENST00000651168.1:c.1075G>A	ENSP00000499074.1:p.Asp359Asn
ENST00000466756.2:c.17G>A
ENST00000473112.6:c.719+808G>A
ENST00000479013.6:c.985G>A	ENSP00000417990.2:p.Asp329Asn
ENST00000481262.6:c.578G>A
ENST00000487418.6:c.1075G>A	ENSP00000418397.2:p.Asp359Asn
ENST00000491554.6:c.463G>A	ENSP00000453146.1:p.Asp155Asn
ENST00000497252.5:n.447G>A
ENST00000497816.1:n.443G>A
ENST00000559575.5:c.29G>A
NM_001159508.1:c.985G>A	NP_001152980.1:p.Asp329Asn
NM_002225.3:c.1075G>A	NP_002216.2:p.Asp359Asn
XM_005254350.2:c.1075G>A	XP_005254407.1:p.Asp359Asn
XM_005254356.2:c.875+808G>A	XP_005254413.1:n.875+808G>A
XM_006720491.2:c.1018G>A	XP_006720554.1:p.Asp340Asn
XM_006720492.2:c.1075G>A	XP_006720555.1:p.Asp359Asn
XM_006720493.2:c.1075G>A	XP_006720556.1:p.Asp359Asn
XM_006720494.2:c.1075G>A	XP_006720557.1:p.Asp359Asn
XM_006720495.2:c.969+808G>A	XP_006720558.1:n.969+808G>A
XM_011521523.1:c.1075G>A	XP_011519825.1:p.Asp359Asn
XR_243097.3:n.981G>A
XR_243098.2:n.981G>A
XR_429453.2:n.1176G>A
NM_001159508.2:c.976G>A	NP_001152980.2:p.Asp326Asn
NM_001354597.2:c.1018G>A	NP_001341526.1:p.Asp340Asn
NM_001354598.2:c.1066G>A	NP_001341527.2:p.Asp356Asn
NM_001354599.2:c.1153G>A	NP_001341528.2:p.Asp385Asn
NM_001354600.2:c.1153G>A	NP_001341529.2:p.Asp385Asn
NM_001354601.2:c.1066G>A	NP_001341530.2:p.Asp356Asn
NM_002225.4:c.1066G>A	NP_002216.3:p.Asp356Asn
NR_148925.1:n.1476G>A
XM_006720495.3:c.969+808G>A	XP_006720558.1:n.969+808G>A
XM_017022149.1:c.1162G>A	XP_016877638.1:p.Asp388Asn
XM_017022150.1:c.1162G>A	XP_016877639.1:p.Asp388Asn
XM_017022153.1:c.1162G>A	XP_016877642.1:p.Asp388Asn
XM_017022154.2:c.1105G>A	XP_016877643.1:p.Asp369Asn
XM_017022155.2:c.1162G>A	XP_016877644.1:p.Asp388Asn
XM_017022157.1:c.1056+808G>A	XP_016877646.1:n.1056+808G>A
XR_001751263.1:n.1425G>A
XR_001751264.1:n.1532G>A
NM_001159508.3:c.976G>A	NP_001152980.2:p.Asp326Asn
NM_001354597.3:c.1018G>A	NP_001341526.1:p.Asp340Asn
NM_001354598.3:c.1066G>A	NP_001341527.2:p.Asp356Asn
NM_001354599.3:c.1153G>A	NP_001341528.2:p.Asp385Asn
NM_001354600.3:c.1153G>A	NP_001341529.2:p.Asp385Asn
NM_001354601.3:c.1066G>A	NP_001341530.2:p.Asp356Asn
NM_002225.5:c.1066G>A MANE Select	NP_002216.3:p.Asp356Asn
NR_148925.2:n.1478G>A