Canonical Allele Identifier: CA2036432530

Gene: KRT86 KRT81

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52306277_52306278delinsAG , CM000674.2:g.52306277_52306278delinsAG	GRCh38
NC_000012.11:g.52700061_52700062delinsAG , CM000674.1:g.52700061_52700062delinsAG	GRCh37
NC_000012.10:g.50986328_50986329delinsAG	NCBI36
NG_008086.1:g.9413_9414delinsAG
NG_008086.2:g.36633_36634delinsAG

Transcript Alleles

HGVS	Amino-acid change
ENST00000423955.7:c.1244_1245delinsAG (KRT86) MANE Select	ENSP00000444533.1:p.Gln415=
ENST00000293525.5:c.1244_1245delinsAG (KRT86)	ENSP00000293525.5:p.Gln415=
ENST00000423955.6:c.1244_1245delinsAG (KRT86)	ENSP00000444533.1:p.Gln415=
NM_002284.3:c.1244_1245delinsAG (KRT86)	NP_002275.1:p.Gln415=
XM_005268866.3:c.1475_1476delinsAG (KRT86)	XP_005268923.1:p.Gln492=
XM_011538334.1:c.-212+1933_-212+1934delinsCT (KRT81)	XP_011536636.1:n.-212+1933_-212+1934delin...
XM_011538336.1:c.1244_1245delinsAG (KRT86)	XP_011536638.1:p.Gln415=
XM_011538337.1:c.1244_1245delinsAG (KRT86)	XP_011536639.1:p.Gln415=
XM_011538338.1:c.1244_1245delinsAG (KRT86)	XP_011536640.1:p.Gln415=
NM_001320198.1:c.1244_1245delinsAG (KRT86)	NP_001307127.1:p.Gln415=
XM_005268866.4:c.1475_1476delinsAG (KRT86)	XP_005268923.1:p.Gln492=
XM_017019296.1:c.1244_1245delinsAG (KRT86)	XP_016874785.1:p.Gln415=
NM_001320198.2:c.1244_1245delinsAG (KRT86) MANE Select	NP_001307127.1:p.Gln415=