Canonical Allele Identifier: CA391717477

Gene: IVD

Linked Data

• MyVariant Identifiers: chr15:g.40703771A>T (hg19) ; chr15:g.40411572A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40411572A>T , CM000677.2:g.40411572A>T	GRCh38
NC_000015.9:g.40703771A>T , CM000677.1:g.40703771A>T	GRCh37
NC_000015.8:g.38491063A>T	NCBI36
NG_011986.1:g.11086A>T
NG_011986.2:g.11088A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000479013.7:c.478A>T	ENSP00000417990.3:p.Asn160Tyr
ENST00000487418.8:c.568A>T MANE Select	ENSP00000418397.3:p.Asn190Tyr
ENST00000650656.1:c.487A>T	ENSP00000498731.1:p.Asn163Tyr
ENST00000651168.1:c.577A>T	ENSP00000499074.1:p.Asn193Tyr
ENST00000473112.6:c.327A>T
ENST00000479013.6:c.487A>T	ENSP00000417990.2:p.Asn163Tyr
ENST00000481262.6:c.174A>T
ENST00000484250.1:n.191A>T
ENST00000487418.6:c.577A>T	ENSP00000418397.2:p.Asn193Tyr
ENST00000558610.5:c.520A>T	ENSP00000453821.1:p.Asn174Tyr
NM_001159508.1:c.487A>T	NP_001152980.1:p.Asn163Tyr
NM_002225.3:c.577A>T	NP_002216.2:p.Asn193Tyr
XM_005254350.2:c.577A>T	XP_005254407.1:p.Asn193Tyr
XM_005254356.2:c.577A>T	XP_005254413.1:p.Asn193Tyr
XM_006720491.2:c.520A>T	XP_006720554.1:p.Asn174Tyr
XM_006720492.2:c.577A>T	XP_006720555.1:p.Asn193Tyr
XM_006720493.2:c.577A>T	XP_006720556.1:p.Asn193Tyr
XM_006720494.2:c.577A>T	XP_006720557.1:p.Asn193Tyr
XM_006720495.2:c.577A>T	XP_006720558.1:p.Asn193Tyr
XM_011521523.1:c.577A>T	XP_011519825.1:p.Asn193Tyr
XM_011521524.1:c.577A>T	XP_011519826.1:p.Asn193Tyr
XR_243097.3:n.577A>T
XR_243098.2:n.577A>T
XR_429453.2:n.678A>T
NM_001159508.2:c.478A>T	NP_001152980.2:p.Asn160Tyr
NM_001354597.2:c.520A>T	NP_001341526.1:p.Asn174Tyr
NM_001354598.2:c.568A>T	NP_001341527.2:p.Asn190Tyr
NM_001354599.2:c.655A>T	NP_001341528.2:p.Asn219Tyr
NM_001354600.2:c.655A>T	NP_001341529.2:p.Asn219Tyr
NM_001354601.2:c.568A>T	NP_001341530.2:p.Asn190Tyr
NM_002225.4:c.568A>T	NP_002216.3:p.Asn190Tyr
NR_148925.1:n.978A>T
XM_006720495.3:c.577A>T	XP_006720558.1:p.Asn193Tyr
XM_017022149.1:c.664A>T	XP_016877638.1:p.Asn222Tyr
XM_017022150.1:c.664A>T	XP_016877639.1:p.Asn222Tyr
XM_017022153.1:c.664A>T	XP_016877642.1:p.Asn222Tyr
XM_017022154.2:c.607A>T	XP_016877643.1:p.Asn203Tyr
XM_017022155.2:c.664A>T	XP_016877644.1:p.Asn222Tyr
XM_017022157.1:c.664A>T	XP_016877646.1:p.Asn222Tyr
XM_017022158.2:c.664A>T	XP_016877647.1:p.Asn222Tyr
XR_001751263.1:n.927A>T
XR_001751264.1:n.968A>T
NM_001159508.3:c.478A>T	NP_001152980.2:p.Asn160Tyr
NM_001354597.3:c.520A>T	NP_001341526.1:p.Asn174Tyr
NM_001354598.3:c.568A>T	NP_001341527.2:p.Asn190Tyr
NM_001354599.3:c.655A>T	NP_001341528.2:p.Asn219Tyr
NM_001354600.3:c.655A>T	NP_001341529.2:p.Asn219Tyr
NM_001354601.3:c.568A>T	NP_001341530.2:p.Asn190Tyr
NM_002225.5:c.568A>T MANE Select	NP_002216.3:p.Asn190Tyr
NR_148925.2:n.980A>T