Canonical Allele Identifier: CA391717743
Gene: IVD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40411627A>T , CM000677.2:g.40411627A>T GRCh38
NC_000015.9:g.40703826A>T , CM000677.1:g.40703826A>T GRCh37
NC_000015.8:g.38491118A>T NCBI36
NG_011986.1:g.11141A>T
NG_011986.2:g.11143A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000479013.7:c.533A>T ENSP00000417990.3:p.Tyr178Phe
ENST00000487418.8:c.623A>T MANE Select ENSP00000418397.3:p.Tyr208Phe
ENST00000650656.1:c.542A>T ENSP00000498731.1:p.Tyr181Phe
ENST00000651168.1:c.632A>T ENSP00000499074.1:p.Tyr211Phe
ENST00000473112.6:c.382A>T
ENST00000479013.6:c.542A>T ENSP00000417990.2:p.Tyr181Phe
ENST00000481262.6:c.229A>T
ENST00000484250.1:n.246A>T
ENST00000487418.6:c.632A>T ENSP00000418397.2:p.Tyr211Phe
ENST00000491554.6:c.20A>T ENSP00000453146.1:p.Tyr7Phe
ENST00000558610.5:c.575A>T ENSP00000453821.1:p.Tyr192Phe
NM_001159508.1:c.542A>T NP_001152980.1:p.Tyr181Phe
NM_002225.3:c.632A>T NP_002216.2:p.Tyr211Phe
XM_005254350.2:c.632A>T XP_005254407.1:p.Tyr211Phe
XM_005254356.2:c.632A>T XP_005254413.1:p.Tyr211Phe
XM_006720491.2:c.575A>T XP_006720554.1:p.Tyr192Phe
XM_006720492.2:c.632A>T XP_006720555.1:p.Tyr211Phe
XM_006720493.2:c.632A>T XP_006720556.1:p.Tyr211Phe
XM_006720494.2:c.632A>T XP_006720557.1:p.Tyr211Phe
XM_006720495.2:c.632A>T XP_006720558.1:p.Tyr211Phe
XM_011521523.1:c.632A>T XP_011519825.1:p.Tyr211Phe
XM_011521524.1:c.632A>T XP_011519826.1:p.Tyr211Phe
XR_243097.3:n.632A>T
XR_243098.2:n.632A>T
XR_429453.2:n.733A>T
NM_001159508.2:c.533A>T NP_001152980.2:p.Tyr178Phe
NM_001354597.2:c.575A>T NP_001341526.1:p.Tyr192Phe
NM_001354598.2:c.623A>T NP_001341527.2:p.Tyr208Phe
NM_001354599.2:c.710A>T NP_001341528.2:p.Tyr237Phe
NM_001354600.2:c.710A>T NP_001341529.2:p.Tyr237Phe
NM_001354601.2:c.623A>T NP_001341530.2:p.Tyr208Phe
NM_002225.4:c.623A>T NP_002216.3:p.Tyr208Phe
NR_148925.1:n.1033A>T
XM_006720495.3:c.632A>T XP_006720558.1:p.Tyr211Phe
XM_017022149.1:c.719A>T XP_016877638.1:p.Tyr240Phe
XM_017022150.1:c.719A>T XP_016877639.1:p.Tyr240Phe
XM_017022153.1:c.719A>T XP_016877642.1:p.Tyr240Phe
XM_017022154.2:c.662A>T XP_016877643.1:p.Tyr221Phe
XM_017022155.2:c.719A>T XP_016877644.1:p.Tyr240Phe
XM_017022157.1:c.719A>T XP_016877646.1:p.Tyr240Phe
XM_017022158.2:c.719A>T XP_016877647.1:p.Tyr240Phe
XR_001751263.1:n.982A>T
XR_001751264.1:n.1023A>T
NM_001159508.3:c.533A>T NP_001152980.2:p.Tyr178Phe
NM_001354597.3:c.575A>T NP_001341526.1:p.Tyr192Phe
NM_001354598.3:c.623A>T NP_001341527.2:p.Tyr208Phe
NM_001354599.3:c.710A>T NP_001341528.2:p.Tyr237Phe
NM_001354600.3:c.710A>T NP_001341529.2:p.Tyr237Phe
NM_001354601.3:c.623A>T NP_001341530.2:p.Tyr208Phe
NM_002225.5:c.623A>T MANE Select NP_002216.3:p.Tyr208Phe
NR_148925.2:n.1035A>T