Canonical Allele Identifier: CA2842863800

Gene: KRT86 KRT81

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52306341dup , CM000674.2:g.52306341dup	GRCh38
NC_000012.11:g.52700125dup , CM000674.1:g.52700125dup	GRCh37
NC_000012.10:g.50986392dup	NCBI36
NG_008086.1:g.9477dup
NG_008086.2:g.36697dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423955.7:c.1247+61dup (KRT86) MANE Select	ENSP00000444533.1:n.1247+61dup
ENST00000293525.5:c.1247+61dup (KRT86)	ENSP00000293525.5:n.1247+61dup
ENST00000423955.6:c.1247+61dup (KRT86)	ENSP00000444533.1:n.1247+61dup
NM_002284.3:c.1247+61dup (KRT86)	NP_002275.1:n.1247+61dup
XM_005268866.3:c.1478+61dup (KRT86)	XP_005268923.1:n.1478+61dup
XM_011538334.1:c.-212+1870dup (KRT81)	XP_011536636.1:n.-212+1870dup
XM_011538336.1:c.1247+61dup (KRT86)	XP_011536638.1:n.1247+61dup
XM_011538337.1:c.1247+61dup (KRT86)	XP_011536639.1:n.1247+61dup
XM_011538338.1:c.1247+61dup (KRT86)	XP_011536640.1:n.1247+61dup
NM_001320198.1:c.1247+61dup (KRT86)	NP_001307127.1:n.1247+61dup
XM_005268866.4:c.1478+61dup (KRT86)	XP_005268923.1:n.1478+61dup
XM_017019296.1:c.1247+61dup (KRT86)	XP_016874785.1:n.1247+61dup
NM_001320198.2:c.1247+61dup (KRT86) MANE Select	NP_001307127.1:n.1247+61dup