Canonical Allele Identifier: CA384919158

Gene: KRT86 KRT81

Linked Data

• MyVariant Identifiers: chr12:g.52699992T>C (hg19) ; chr12:g.52306208T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52306208T>C , CM000674.2:g.52306208T>C	GRCh38
NC_000012.11:g.52699992T>C , CM000674.1:g.52699992T>C	GRCh37
NC_000012.10:g.50986259T>C	NCBI36
NG_008086.1:g.9344T>C
NG_008086.2:g.36564T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423955.7:c.1175T>C (KRT86) MANE Select	ENSP00000444533.1:p.Val392Ala
ENST00000293525.5:c.1175T>C (KRT86)	ENSP00000293525.5:p.Val392Ala
ENST00000423955.6:c.1175T>C (KRT86)	ENSP00000444533.1:p.Val392Ala
NM_002284.3:c.1175T>C (KRT86)	NP_002275.1:p.Val392Ala
XM_005268866.3:c.1406T>C (KRT86)	XP_005268923.1:p.Val469Ala
XM_011538334.1:c.-212+2003A>G (KRT81)	XP_011536636.1:n.-212+2003A>G
XM_011538336.1:c.1175T>C (KRT86)	XP_011536638.1:p.Val392Ala
XM_011538337.1:c.1175T>C (KRT86)	XP_011536639.1:p.Val392Ala
XM_011538338.1:c.1175T>C (KRT86)	XP_011536640.1:p.Val392Ala
NM_001320198.1:c.1175T>C (KRT86)	NP_001307127.1:p.Val392Ala
XM_005268866.4:c.1406T>C (KRT86)	XP_005268923.1:p.Val469Ala
XM_017019296.1:c.1175T>C (KRT86)	XP_016874785.1:p.Val392Ala
NM_001320198.2:c.1175T>C (KRT86) MANE Select	NP_001307127.1:p.Val392Ala