Canonical Allele Identifier: CA2036432482

Gene: KRT86 KRT81

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52306175A= , CM000674.2:g.52306175A=	GRCh38
NC_000012.11:g.52699959A= , CM000674.1:g.52699959A=	GRCh37
NC_000012.10:g.50986226A=	NCBI36
NG_008086.1:g.9311A=
NG_008086.2:g.36531A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000423955.7:c.1142A= (KRT86) MANE Select	ENSP00000444533.1:p.Asp381=
ENST00000293525.5:c.1142A= (KRT86)	ENSP00000293525.5:p.Asp381=
ENST00000423955.6:c.1142A= (KRT86)	ENSP00000444533.1:p.Asp381=
NM_002284.3:c.1142A= (KRT86)	NP_002275.1:p.Asp381=
XM_005268866.3:c.1373A= (KRT86)	XP_005268923.1:p.Asp458=
XM_011538334.1:c.-212+2036T= (KRT81)	XP_011536636.1:n.-212+2036T=
XM_011538336.1:c.1142A= (KRT86)	XP_011536638.1:p.Asp381=
XM_011538337.1:c.1142A= (KRT86)	XP_011536639.1:p.Asp381=
XM_011538338.1:c.1142A= (KRT86)	XP_011536640.1:p.Asp381=
NM_001320198.1:c.1142A= (KRT86)	NP_001307127.1:p.Asp381=
XM_005268866.4:c.1373A= (KRT86)	XP_005268923.1:p.Asp458=
XM_017019296.1:c.1142A= (KRT86)	XP_016874785.1:p.Asp381=
NM_001320198.2:c.1142A= (KRT86) MANE Select	NP_001307127.1:p.Asp381=