Canonical Allele Identifier: CA2036418311

Gene: KRT86 KRT81

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52285934_52285936delinsAAC , CM000674.2:g.52285934_52285936delinsAAC	GRCh38
NC_000012.11:g.52679718_52679720delinsAAC , CM000674.1:g.52679718_52679720delinsAAC	GRCh37
NC_000012.10:g.50965985_50965987delinsAAC	NCBI36
NG_008184.1:g.10580_10582delinsGTT
NG_008086.2:g.16290_16292delinsAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423955.7:c.-5+9988_-5+9990delinsAAC (KRT86) MANE Select	ENSP00000444533.1:n.-5+9988_-5+9990delinsAAC
ENST00000327741.9:c.*319_*321delinsGTT (KRT81) MANE Select	ENSP00000369349.4:n.*319_*321delinsGTT
ENST00000423955.6:c.-5+9988_-5+9990delinsAAC (KRT86)	ENSP00000444533.1:n.-5+9988_-5+9990delinsAAC
ENST00000553310.6:c.-4-15979_-4-15977delinsAAC (KRT86)	ENSP00000452237.3:n.-4-15979_-4-15977delinsAAC
NM_002281.3:c.*319_*321delinsGTT (KRT81)	NP_002272.2:n.*319_*321delinsGTT
XM_005268866.3:c.129+9988_129+9990delinsAAC (KRT86)	XP_005268923.1:n.129+9988_129+9990delinsAAC
XM_011538334.1:c.*319_*321delinsGTT (KRT81)	XP_011536636.1:n.*319_*321delinsGTT
XM_011538336.1:c.-5+9988_-5+9990delinsAAC (KRT86)	XP_011536638.1:n.-5+9988_-5+9990delinsAAC
XM_011538337.1:c.-5+9988_-5+9990delinsAAC (KRT86)	XP_011536639.1:n.-5+9988_-5+9990delinsAAC
XM_011538338.1:c.-5+9988_-5+9990delinsAAC (KRT86)	XP_011536640.1:n.-5+9988_-5+9990delinsAAC
NM_001320198.1:c.-5+9988_-5+9990delinsAAC (KRT86)	NP_001307127.1:n.-5+9988_-5+9990delinsAAC
XM_005268866.4:c.129+9988_129+9990delinsAAC (KRT86)	XP_005268923.1:n.129+9988_129+9990delinsAAC
XM_017019296.1:c.-103+9988_-103+9990delinsAAC (KRT86)	XP_016874785.1:n.-103+9988_-103+9990delinsAAC
NM_001320198.2:c.-5+9988_-5+9990delinsAAC (KRT86) MANE Select	NP_001307127.1:n.-5+9988_-5+9990delinsAAC
NM_002281.4:c.*319_*321delinsGTT (KRT81) MANE Select	NP_002272.2:n.*319_*321delinsGTT