Canonical Allele Identifier: CA2036418607

Gene: KRT86 KRT81

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52286273_52286274delinsGC , CM000674.2:g.52286273_52286274delinsGC	GRCh38
NC_000012.11:g.52680057_52680058delinsGC , CM000674.1:g.52680057_52680058delinsGC	GRCh37
NC_000012.10:g.50966324_50966325delinsGC	NCBI36
NG_008184.1:g.10242_10243delinsGC
NG_008086.2:g.16629_16630delinsGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423955.7:c.-5+10327_-5+10328delinsGC (KRT86) MANE Select	ENSP00000444533.1:n.-5+10327_-5+10328delinsGC
ENST00000327741.9:c.1499_1500delinsGC (KRT81) MANE Select	ENSP00000369349.4:p.Ser500=
ENST00000423955.6:c.-5+10327_-5+10328delinsGC (KRT86)	ENSP00000444533.1:n.-5+10327_-5+10328delinsGC
ENST00000553310.6:c.-4-15640_-4-15639delinsGC (KRT86)	ENSP00000452237.3:n.-4-15640_-4-15639delinsGC
ENST00000615839.1:c.1436_1437delinsGC (KRT81)	ENSP00000483796.1:p.Ser479=
NM_002281.3:c.1499_1500delinsGC (KRT81)	NP_002272.2:p.Ser500=
XM_005268866.3:c.129+10327_129+10328delinsGC (KRT86)	XP_005268923.1:n.129+10327_129+10328delinsGC
XM_011538334.1:c.1499_1500delinsGC (KRT81)	XP_011536636.1:p.Ser500=
XM_011538336.1:c.-5+10327_-5+10328delinsGC (KRT86)	XP_011536638.1:n.-5+10327_-5+10328delinsGC
XM_011538337.1:c.-5+10327_-5+10328delinsGC (KRT86)	XP_011536639.1:n.-5+10327_-5+10328delinsGC
XM_011538338.1:c.-5+10327_-5+10328delinsGC (KRT86)	XP_011536640.1:n.-5+10327_-5+10328delinsGC
NM_001320198.1:c.-5+10327_-5+10328delinsGC (KRT86)	NP_001307127.1:n.-5+10327_-5+10328delinsGC
XM_005268866.4:c.129+10327_129+10328delinsGC (KRT86)	XP_005268923.1:n.129+10327_129+10328delinsGC
XM_017019296.1:c.-103+10327_-103+10328delinsGC (KRT86)	XP_016874785.1:n.-103+10327_-103+10328delinsGC
NM_001320198.2:c.-5+10327_-5+10328delinsGC (KRT86) MANE Select	NP_001307127.1:n.-5+10327_-5+10328delinsGC
NM_002281.4:c.1499_1500delinsGC (KRT81) MANE Select	NP_002272.2:p.Ser500=