Canonical Allele Identifier: CA391745110
Gene: IVD HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.40407779C>A , CM000677.2:g.40407779C>A GRCh38
NC_000015.9:g.40699980C>A , CM000677.1:g.40699980C>A GRCh37
NC_000015.8:g.38487272C>A NCBI36
NG_011986.1:g.7295C>A
NG_011986.2:g.7295C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000479013.7:c.145-160C>A ENSP00000417990.3:n.145-160C>A
ENST00000487418.8:c.234+54C>A MANE Select ENSP00000418397.3:n.234+54C>A
ENST00000610693.5:c.288C>A ENSP00000479359.2:p.Cys96Ter
ENST00000650656.1:c.154-160C>A ENSP00000498731.1:n.154-160C>A
ENST00000651168.1:c.243+54C>A ENSP00000499074.1:n.243+54C>A
ENST00000479013.6:c.154-160C>A ENSP00000417990.2:n.154-160C>A
ENST00000487418.6:c.243+54C>A ENSP00000418397.2:n.243+54C>A
ENST00000558610.5:c.186+54C>A ENSP00000453821.1:n.186+54C>A
ENST00000610693.4:c.297C>A ENSP00000479359.1:p.Cys99Ter
NM_001159508.1:c.154-160C>A NP_001152980.1:n.154-160C>A
NM_002225.3:c.243+54C>A NP_002216.2:n.243+54C>A
XM_005254350.2:c.243+54C>A XP_005254407.1:n.243+54C>A
XM_005254356.2:c.243+54C>A XP_005254413.1:n.243+54C>A
XM_006720491.2:c.186+54C>A XP_006720554.1:n.186+54C>A
XM_006720492.2:c.243+54C>A XP_006720555.1:n.243+54C>A
XM_006720493.2:c.243+54C>A XP_006720556.1:n.243+54C>A
XM_006720494.2:c.243+54C>A XP_006720557.1:n.243+54C>A
XM_006720495.2:c.243+54C>A XP_006720558.1:n.243+54C>A
XM_011521523.1:c.243+54C>A XP_011519825.1:n.243+54C>A
XM_011521524.1:c.243+54C>A XP_011519826.1:n.243+54C>A
XR_243097.3:n.243+54C>A
XR_243098.2:n.243+54C>A
XR_429453.2:n.344+54C>A
NM_001159508.2:c.145-160C>A NP_001152980.2:n.145-160C>A
NM_001354597.2:c.186+54C>A NP_001341526.1:n.186+54C>A
NM_001354598.2:c.234+54C>A NP_001341527.2:n.234+54C>A
NM_001354599.2:c.288C>A NP_001341528.2:p.Cys96Ter
NM_001354600.2:c.288C>A NP_001341529.2:p.Cys96Ter
NM_001354601.2:c.234+54C>A NP_001341530.2:n.234+54C>A
NM_002225.4:c.234+54C>A NP_002216.3:n.234+54C>A
NR_148925.1:n.644+54C>A
XM_006720495.3:c.243+54C>A XP_006720558.1:n.243+54C>A
XM_017022149.1:c.297C>A XP_016877638.1:p.Cys99Ter
XM_017022150.1:c.297C>A XP_016877639.1:p.Cys99Ter
XM_017022153.1:c.297C>A XP_016877642.1:p.Cys99Ter
XM_017022154.2:c.240C>A XP_016877643.1:p.Cys80Ter
XM_017022155.2:c.297C>A XP_016877644.1:p.Cys99Ter
XM_017022157.1:c.297C>A XP_016877646.1:p.Cys99Ter
XM_017022158.2:c.297C>A XP_016877647.1:p.Cys99Ter
XR_001751263.1:n.593+54C>A
XR_001751264.1:n.634+54C>A
NM_001159508.3:c.145-160C>A NP_001152980.2:n.145-160C>A
NM_001354597.3:c.186+54C>A NP_001341526.1:n.186+54C>A
NM_001354598.3:c.234+54C>A NP_001341527.2:n.234+54C>A
NM_001354599.3:c.288C>A NP_001341528.2:p.Cys96Ter
NM_001354600.3:c.288C>A NP_001341529.2:p.Cys96Ter
NM_001354601.3:c.234+54C>A NP_001341530.2:n.234+54C>A
NM_002225.5:c.234+54C>A MANE Select NP_002216.3:n.234+54C>A
NR_148925.2:n.646+54C>A