Canonical Allele Identifier: CA2036418630

Gene: KRT86 KRT81

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52286290C= , CM000674.2:g.52286290C=	GRCh38
NC_000012.11:g.52680074C= , CM000674.1:g.52680074C=	GRCh37
NC_000012.10:g.50966341C=	NCBI36
NG_008184.1:g.10226G=
NG_008086.2:g.16646C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423955.7:c.-5+10344C= (KRT86) MANE Select	ENSP00000444533.1:n.-5+10344C=
ENST00000327741.9:c.1483G= (KRT81) MANE Select	ENSP00000369349.4:p.Val495=
ENST00000423955.6:c.-5+10344C= (KRT86)	ENSP00000444533.1:n.-5+10344C=
ENST00000553310.6:c.-4-15623C= (KRT86)	ENSP00000452237.3:n.-4-15623C=
ENST00000615839.1:c.1420G= (KRT81)	ENSP00000483796.1:p.Val474=
NM_002281.3:c.1483G= (KRT81)	NP_002272.2:p.Val495=
XM_005268866.3:c.129+10344C= (KRT86)	XP_005268923.1:n.129+10344C=
XM_011538334.1:c.1483G= (KRT81)	XP_011536636.1:p.Val495=
XM_011538336.1:c.-5+10344C= (KRT86)	XP_011536638.1:n.-5+10344C=
XM_011538337.1:c.-5+10344C= (KRT86)	XP_011536639.1:n.-5+10344C=
XM_011538338.1:c.-5+10344C= (KRT86)	XP_011536640.1:n.-5+10344C=
NM_001320198.1:c.-5+10344C= (KRT86)	NP_001307127.1:n.-5+10344C=
XM_005268866.4:c.129+10344C= (KRT86)	XP_005268923.1:n.129+10344C=
XM_017019296.1:c.-103+10344C= (KRT86)	XP_016874785.1:n.-103+10344C=
NM_001320198.2:c.-5+10344C= (KRT86) MANE Select	NP_001307127.1:n.-5+10344C=
NM_002281.4:c.1483G= (KRT81) MANE Select	NP_002272.2:p.Val495=