Canonical Allele Identifier: CA2036418624

Gene: KRT86 KRT81

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52286284_52286285delinsAC , CM000674.2:g.52286284_52286285delinsAC	GRCh38
NC_000012.11:g.52680068_52680069delinsAC , CM000674.1:g.52680068_52680069delinsAC	GRCh37
NC_000012.10:g.50966335_50966336delinsAC	NCBI36
NG_008184.1:g.10231_10232delinsGT
NG_008086.2:g.16640_16641delinsAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423955.7:c.-5+10338_-5+10339delinsAC (KRT86) MANE Select	ENSP00000444533.1:n.-5+10338_-5+10339delinsAC
ENST00000327741.9:c.1488_1489delinsGT (KRT81) MANE Select	ENSP00000369349.4:p.Gly496=
ENST00000423955.6:c.-5+10338_-5+10339delinsAC (KRT86)	ENSP00000444533.1:n.-5+10338_-5+10339delinsAC
ENST00000553310.6:c.-4-15629_-4-15628delinsAC (KRT86)	ENSP00000452237.3:n.-4-15629_-4-15628delinsAC
ENST00000615839.1:c.1425_1426delinsGT (KRT81)	ENSP00000483796.1:p.Gly475=
NM_002281.3:c.1488_1489delinsGT (KRT81)	NP_002272.2:p.Gly496=
XM_005268866.3:c.129+10338_129+10339delinsAC (KRT86)	XP_005268923.1:n.129+10338_129+10339delinsAC
XM_011538334.1:c.1488_1489delinsGT (KRT81)	XP_011536636.1:p.Gly496=
XM_011538336.1:c.-5+10338_-5+10339delinsAC (KRT86)	XP_011536638.1:n.-5+10338_-5+10339delinsAC
XM_011538337.1:c.-5+10338_-5+10339delinsAC (KRT86)	XP_011536639.1:n.-5+10338_-5+10339delinsAC
XM_011538338.1:c.-5+10338_-5+10339delinsAC (KRT86)	XP_011536640.1:n.-5+10338_-5+10339delinsAC
NM_001320198.1:c.-5+10338_-5+10339delinsAC (KRT86)	NP_001307127.1:n.-5+10338_-5+10339delinsAC
XM_005268866.4:c.129+10338_129+10339delinsAC (KRT86)	XP_005268923.1:n.129+10338_129+10339delinsAC
XM_017019296.1:c.-103+10338_-103+10339delinsAC (KRT86)	XP_016874785.1:n.-103+10338_-103+10339delinsAC
NM_001320198.2:c.-5+10338_-5+10339delinsAC (KRT86) MANE Select	NP_001307127.1:n.-5+10338_-5+10339delinsAC
NM_002281.4:c.1488_1489delinsGT (KRT81) MANE Select	NP_002272.2:p.Gly496=