Canonical Allele Identifier: CA2575163144

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52286249_52286253del , CM000674.2:g.52286249_52286253del GRCh38
NC_000012.11:g.52680033_52680037del , CM000674.1:g.52680033_52680037del GRCh37
NC_000012.10:g.50966300_50966304del NCBI36
NG_008184.1:g.10265_10269del
NG_008086.2:g.16605_16609del

Transcript Alleles

HGVS Amino-acid Change
ENST00000423955.7:c.-5+10303_-5+10307del (KRT86) MANE Select ENSP00000444533.1:n.-5+10303_-5+10307del
ENST00000327741.9:c.*4_*8del (KRT81) MANE Select ENSP00000369349.4:n.*4_*8del
ENST00000423955.6:c.-5+10303_-5+10307del (KRT86) ENSP00000444533.1:n.-5+10303_-5+10307del
ENST00000553310.6:c.-4-15664_-4-15660del (KRT86) ENSP00000452237.3:n.-4-15664_-4-15660del
NM_002281.3:c.*4_*8del (KRT81) NP_002272.2:n.*4_*8del
XM_005268866.3:c.129+10303_129+10307del (KRT86) XP_005268923.1:n.129+10303_129+10307del
XM_011538334.1:c.*4_*8del (KRT81) XP_011536636.1:n.*4_*8del
XM_011538336.1:c.-5+10303_-5+10307del (KRT86) XP_011536638.1:n.-5+10303_-5+10307del
XM_011538337.1:c.-5+10303_-5+10307del (KRT86) XP_011536639.1:n.-5+10303_-5+10307del
XM_011538338.1:c.-5+10303_-5+10307del (KRT86) XP_011536640.1:n.-5+10303_-5+10307del
NM_001320198.1:c.-5+10303_-5+10307del (KRT86) NP_001307127.1:n.-5+10303_-5+10307del
XM_005268866.4:c.129+10303_129+10307del (KRT86) XP_005268923.1:n.129+10303_129+10307del
XM_017019296.1:c.-103+10303_-103+10307del (KRT86) XP_016874785.1:n.-103+10303_-103+10307del
NM_001320198.2:c.-5+10303_-5+10307del (KRT86) MANE Select NP_001307127.1:n.-5+10303_-5+10307del
NM_002281.4:c.*4_*8del (KRT81) MANE Select NP_002272.2:n.*4_*8del