Canonical Allele Identifier: CA2036418203

Gene: KRT86

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52285830_52285831delinsCT , CM000674.2:g.52285830_52285831delinsCT	GRCh38
NC_000012.11:g.52679614_52679615delinsCT , CM000674.1:g.52679614_52679615delinsCT	GRCh37
NC_000012.10:g.50965881_50965882delinsCT	NCBI36
NG_008184.1:g.10685_10686delinsAG
NG_008086.2:g.16186_16187delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423955.7:c.-5+9884_-5+9885delinsCT MANE Select	ENSP00000444533.1:n.-5+9884_-5+9885delinsCT
ENST00000423955.6:c.-5+9884_-5+9885delinsCT	ENSP00000444533.1:n.-5+9884_-5+9885delinsCT
ENST00000553310.6:c.-4-16083_-4-16082delinsCT	ENSP00000452237.3:n.-4-16083_-4-16082delinsCT
XM_005268866.3:c.129+9884_129+9885delinsCT	XP_005268923.1:n.129+9884_129+9885delinsCT
XM_011538336.1:c.-5+9884_-5+9885delinsCT	XP_011536638.1:n.-5+9884_-5+9885delinsCT
XM_011538337.1:c.-5+9884_-5+9885delinsCT	XP_011536639.1:n.-5+9884_-5+9885delinsCT
XM_011538338.1:c.-5+9884_-5+9885delinsCT	XP_011536640.1:n.-5+9884_-5+9885delinsCT
NM_001320198.1:c.-5+9884_-5+9885delinsCT	NP_001307127.1:n.-5+9884_-5+9885delinsCT
XM_005268866.4:c.129+9884_129+9885delinsCT	XP_005268923.1:n.129+9884_129+9885delinsCT
XM_017019296.1:c.-103+9884_-103+9885delinsCT	XP_016874785.1:n.-103+9884_-103+9885delinsCT
NM_001320198.2:c.-5+9884_-5+9885delinsCT MANE Select	NP_001307127.1:n.-5+9884_-5+9885delinsCT