Canonical Allele Identifier: CA623580354

Linked Data

dbSNP Id: rs1567585252

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.72060432_72060434del , CM000678.2:g.72060432_72060434del GRCh38
NC_000016.9:g.72094331_72094333del , CM000678.1:g.72094331_72094333del GRCh37
NC_000016.8:g.70651832_70651834del NCBI36
NG_012651.1:g.10824_10826del
NG_030311.1:g.2207_2209del

Transcript Alleles

HGVS Amino-acid Change
ENST00000355906.10:c.763_765del (HP) MANE Select ENSP00000348170.5:p.Lys255del
ENST00000228226.12:c.388_390del (HP) ENSP00000228226.9:p.Lys130del
ENST00000355906.9:c.763_765del (HP) ENSP00000348170.5:p.Lys255del
ENST00000357763.8:c.871_873del (HP) ENSP00000350406.5:p.Lys291del
ENST00000398131.6:c.586_588del (HP) ENSP00000381199.2:p.Lys196del
ENST00000562153.5:c.285-16075_285-16073del (TXNL4B) ENSP00000454635.1:n.285-16075_285-16073del
ENST00000562526.5:c.266-231_266-229del (HP) ENSP00000454413.1:n.266-231_266-229del
ENST00000564499.5:c.466_468del (HP) ENSP00000456503.1:p.Lys156del
ENST00000565574.5:c.586_588del (HP) ENSP00000454966.1:p.Lys196del
ENST00000566821.1:n.2402_2404del (HP)
ENST00000567185.7:c.755_757del (HP)
ENST00000567612.2:c.638_640del (HP)
ENST00000570083.5:c.586_588del (HP) ENSP00000457629.1:p.Lys196del
ENST00000613898.1:c.388_390del (HP) ENSP00000478279.1:p.Lys130del
NM_001126102.1:c.586_588del (HP) NP_001119574.1:p.Lys196del
NM_005143.3:c.763_765del (HP) NP_005134.1:p.Lys255del
XM_005255922.3:c.586_588del (HP) XP_005255979.2:p.Lys196del
NM_001126102.2:c.586_588del (HP) NP_001119574.1:p.Lys196del
NM_001318138.1:c.586_588del (HP) NP_001305067.1:p.Lys196del
NM_005143.4:c.763_765del (HP) NP_005134.1:p.Lys255del
XM_017023377.2:c.285-16075_285-16073del (TXNL4B) XP_016878866.1:n.285-16075_285-16073del
NM_001318138.2:c.586_588del (HP) NP_001305067.1:p.Lys196del
NM_005143.5:c.763_765del (HP) MANE Select NP_005134.1:p.Lys255del
NM_001126102.3:c.586_588del (HP) NP_001119574.1:p.Lys196del