Canonical Allele Identifier: CA384913262

Gene: KRT86 KRT81

Linked Data

• gnomAD v4: 12-52286272-T-C
• MyVariant Identifiers: chr12:g.52680056T>C (hg19) ; chr12:g.52286272T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52286272T>C , CM000674.2:g.52286272T>C	GRCh38
NC_000012.11:g.52680056T>C , CM000674.1:g.52680056T>C	GRCh37
NC_000012.10:g.50966323T>C	NCBI36
NG_008184.1:g.10244A>G
NG_008086.2:g.16628T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423955.7:c.-5+10326T>C (KRT86) MANE Select	ENSP00000444533.1:n.-5+10326T>C
ENST00000327741.9:c.1501A>G (KRT81) MANE Select	ENSP00000369349.4:p.Ser501Gly
ENST00000423955.6:c.-5+10326T>C (KRT86)	ENSP00000444533.1:n.-5+10326T>C
ENST00000553310.6:c.-4-15641T>C (KRT86)	ENSP00000452237.3:n.-4-15641T>C
ENST00000615839.1:c.1438A>G (KRT81)	ENSP00000483796.1:p.Ser480Gly
NM_002281.3:c.1501A>G (KRT81)	NP_002272.2:p.Ser501Gly
XM_005268866.3:c.129+10326T>C (KRT86)	XP_005268923.1:n.129+10326T>C
XM_011538334.1:c.1501A>G (KRT81)	XP_011536636.1:p.Ser501Gly
XM_011538336.1:c.-5+10326T>C (KRT86)	XP_011536638.1:n.-5+10326T>C
XM_011538337.1:c.-5+10326T>C (KRT86)	XP_011536639.1:n.-5+10326T>C
XM_011538338.1:c.-5+10326T>C (KRT86)	XP_011536640.1:n.-5+10326T>C
NM_001320198.1:c.-5+10326T>C (KRT86)	NP_001307127.1:n.-5+10326T>C
XM_005268866.4:c.129+10326T>C (KRT86)	XP_005268923.1:n.129+10326T>C
XM_017019296.1:c.-103+10326T>C (KRT86)	XP_016874785.1:n.-103+10326T>C
NM_001320198.2:c.-5+10326T>C (KRT86) MANE Select	NP_001307127.1:n.-5+10326T>C
NM_002281.4:c.1501A>G (KRT81) MANE Select	NP_002272.2:p.Ser501Gly