Canonical Allele Identifier: CA2036418091

Gene: KRT86

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52285716T= , CM000674.2:g.52285716T=	GRCh38
NC_000012.11:g.52679500T= , CM000674.1:g.52679500T=	GRCh37
NC_000012.10:g.50965767T=	NCBI36
NG_008184.1:g.10800A=
NG_008086.2:g.16072T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423955.7:c.-5+9770T= MANE Select	ENSP00000444533.1:n.-5+9770T=
ENST00000423955.6:c.-5+9770T=	ENSP00000444533.1:n.-5+9770T=
ENST00000553310.6:c.-4-16197T=	ENSP00000452237.3:n.-4-16197T=
XM_005268866.3:c.129+9770T=	XP_005268923.1:n.129+9770T=
XM_011538336.1:c.-5+9770T=	XP_011536638.1:n.-5+9770T=
XM_011538337.1:c.-5+9770T=	XP_011536639.1:n.-5+9770T=
XM_011538338.1:c.-5+9770T=	XP_011536640.1:n.-5+9770T=
NM_001320198.1:c.-5+9770T=	NP_001307127.1:n.-5+9770T=
XM_005268866.4:c.129+9770T=	XP_005268923.1:n.129+9770T=
XM_017019296.1:c.-103+9770T=	XP_016874785.1:n.-103+9770T=
NM_001320198.2:c.-5+9770T= MANE Select	NP_001307127.1:n.-5+9770T=