Canonical Allele Identifier: CA2618897608

Gene: KRT86 KRT81

Linked Data

• gnomAD v4: 12-52286077-TG-T

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52286081del , CM000674.2:g.52286081del	GRCh38
NC_000012.11:g.52679865del , CM000674.1:g.52679865del	GRCh37
NC_000012.10:g.50966132del	NCBI36
NG_008184.1:g.10438del
NG_008086.2:g.16437del

Transcript Alleles

HGVS	Amino-acid change
ENST00000423955.7:c.-5+10135del (KRT86) MANE Select	ENSP00000444533.1:n.-5+10135del
ENST00000327741.9:c.*177del (KRT81) MANE Select	ENSP00000369349.4:n.*177del
ENST00000423955.6:c.-5+10135del (KRT86)	ENSP00000444533.1:n.-5+10135del
ENST00000553310.6:c.-4-15832del (KRT86)	ENSP00000452237.3:n.-4-15832del
NM_002281.3:c.*177del (KRT81)	NP_002272.2:n.*177del
XM_005268866.3:c.129+10135del (KRT86)	XP_005268923.1:n.129+10135del
XM_011538334.1:c.*177del (KRT81)	XP_011536636.1:n.*177del
XM_011538336.1:c.-5+10135del (KRT86)	XP_011536638.1:n.-5+10135del
XM_011538337.1:c.-5+10135del (KRT86)	XP_011536639.1:n.-5+10135del
XM_011538338.1:c.-5+10135del (KRT86)	XP_011536640.1:n.-5+10135del
NM_001320198.1:c.-5+10135del (KRT86)	NP_001307127.1:n.-5+10135del
XM_005268866.4:c.129+10135del (KRT86)	XP_005268923.1:n.129+10135del
XM_017019296.1:c.-103+10135del (KRT86)	XP_016874785.1:n.-103+10135del
NM_001320198.2:c.-5+10135del (KRT86) MANE Select	NP_001307127.1:n.-5+10135del
NM_002281.4:c.*177del (KRT81) MANE Select	NP_002272.2:n.*177del