Canonical Allele Identifier: CA391717459
Gene: IVD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40411568C>G , CM000677.2:g.40411568C>G GRCh38
NC_000015.9:g.40703767C>G , CM000677.1:g.40703767C>G GRCh37
NC_000015.8:g.38491059C>G NCBI36
NG_011986.1:g.11082C>G
NG_011986.2:g.11084C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000479013.7:c.474C>G ENSP00000417990.3:p.Ile158Met
ENST00000487418.8:c.564C>G MANE Select ENSP00000418397.3:p.Ile188Met
ENST00000650656.1:c.483C>G ENSP00000498731.1:p.Ile161Met
ENST00000651168.1:c.573C>G ENSP00000499074.1:p.Ile191Met
ENST00000473112.6:c.323C>G
ENST00000479013.6:c.483C>G ENSP00000417990.2:p.Ile161Met
ENST00000481262.6:c.170C>G
ENST00000484250.1:n.187C>G
ENST00000487418.6:c.573C>G ENSP00000418397.2:p.Ile191Met
ENST00000558610.5:c.516C>G ENSP00000453821.1:p.Ile172Met
NM_001159508.1:c.483C>G NP_001152980.1:p.Ile161Met
NM_002225.3:c.573C>G NP_002216.2:p.Ile191Met
XM_005254350.2:c.573C>G XP_005254407.1:p.Ile191Met
XM_005254356.2:c.573C>G XP_005254413.1:p.Ile191Met
XM_006720491.2:c.516C>G XP_006720554.1:p.Ile172Met
XM_006720492.2:c.573C>G XP_006720555.1:p.Ile191Met
XM_006720493.2:c.573C>G XP_006720556.1:p.Ile191Met
XM_006720494.2:c.573C>G XP_006720557.1:p.Ile191Met
XM_006720495.2:c.573C>G XP_006720558.1:p.Ile191Met
XM_011521523.1:c.573C>G XP_011519825.1:p.Ile191Met
XM_011521524.1:c.573C>G XP_011519826.1:p.Ile191Met
XR_243097.3:n.573C>G
XR_243098.2:n.573C>G
XR_429453.2:n.674C>G
NM_001159508.2:c.474C>G NP_001152980.2:p.Ile158Met
NM_001354597.2:c.516C>G NP_001341526.1:p.Ile172Met
NM_001354598.2:c.564C>G NP_001341527.2:p.Ile188Met
NM_001354599.2:c.651C>G NP_001341528.2:p.Ile217Met
NM_001354600.2:c.651C>G NP_001341529.2:p.Ile217Met
NM_001354601.2:c.564C>G NP_001341530.2:p.Ile188Met
NM_002225.4:c.564C>G NP_002216.3:p.Ile188Met
NR_148925.1:n.974C>G
XM_006720495.3:c.573C>G XP_006720558.1:p.Ile191Met
XM_017022149.1:c.660C>G XP_016877638.1:p.Ile220Met
XM_017022150.1:c.660C>G XP_016877639.1:p.Ile220Met
XM_017022153.1:c.660C>G XP_016877642.1:p.Ile220Met
XM_017022154.2:c.603C>G XP_016877643.1:p.Ile201Met
XM_017022155.2:c.660C>G XP_016877644.1:p.Ile220Met
XM_017022157.1:c.660C>G XP_016877646.1:p.Ile220Met
XM_017022158.2:c.660C>G XP_016877647.1:p.Ile220Met
XR_001751263.1:n.923C>G
XR_001751264.1:n.964C>G
NM_001159508.3:c.474C>G NP_001152980.2:p.Ile158Met
NM_001354597.3:c.516C>G NP_001341526.1:p.Ile172Met
NM_001354598.3:c.564C>G NP_001341527.2:p.Ile188Met
NM_001354599.3:c.651C>G NP_001341528.2:p.Ile217Met
NM_001354600.3:c.651C>G NP_001341529.2:p.Ile217Met
NM_001354601.3:c.564C>G NP_001341530.2:p.Ile188Met
NM_002225.5:c.564C>G MANE Select NP_002216.3:p.Ile188Met
NR_148925.2:n.976C>G