Canonical Allele Identifier: CA2618897546

Gene: KRT86 KRT81

Linked Data

• gnomAD v4: 12-52286054-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52286054T>G , CM000674.2:g.52286054T>G	GRCh38
NC_000012.11:g.52679838T>G , CM000674.1:g.52679838T>G	GRCh37
NC_000012.10:g.50966105T>G	NCBI36
NG_008184.1:g.10462A>C
NG_008086.2:g.16410T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000423955.7:c.-5+10108T>G (KRT86) MANE Select	ENSP00000444533.1:n.-5+10108T>G
ENST00000327741.9:c.*201A>C (KRT81) MANE Select	ENSP00000369349.4:n.*201A>C
ENST00000423955.6:c.-5+10108T>G (KRT86)	ENSP00000444533.1:n.-5+10108T>G
ENST00000553310.6:c.-4-15859T>G (KRT86)	ENSP00000452237.3:n.-4-15859T>G
NM_002281.3:c.*201A>C (KRT81)	NP_002272.2:n.*201A>C
XM_005268866.3:c.129+10108T>G (KRT86)	XP_005268923.1:n.129+10108T>G
XM_011538334.1:c.*201A>C (KRT81)	XP_011536636.1:n.*201A>C
XM_011538336.1:c.-5+10108T>G (KRT86)	XP_011536638.1:n.-5+10108T>G
XM_011538337.1:c.-5+10108T>G (KRT86)	XP_011536639.1:n.-5+10108T>G
XM_011538338.1:c.-5+10108T>G (KRT86)	XP_011536640.1:n.-5+10108T>G
NM_001320198.1:c.-5+10108T>G (KRT86)	NP_001307127.1:n.-5+10108T>G
XM_005268866.4:c.129+10108T>G (KRT86)	XP_005268923.1:n.129+10108T>G
XM_017019296.1:c.-103+10108T>G (KRT86)	XP_016874785.1:n.-103+10108T>G
NM_001320198.2:c.-5+10108T>G (KRT86) MANE Select	NP_001307127.1:n.-5+10108T>G
NM_002281.4:c.*201A>C (KRT81) MANE Select	NP_002272.2:n.*201A>C