Canonical Allele Identifier: CA2726050956

Gene: KRT86

Linked Data

• dbSNP Id: rs79978767

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52285868C>G , CM000674.2:g.52285868C>G	GRCh38
NC_000012.11:g.52679652C>G , CM000674.1:g.52679652C>G	GRCh37
NC_000012.10:g.50965919C>G	NCBI36
NG_008184.1:g.10648G>C
NG_008086.2:g.16224C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423955.7:c.-5+9922C>G MANE Select	ENSP00000444533.1:n.-5+9922C>G
ENST00000423955.6:c.-5+9922C>G	ENSP00000444533.1:n.-5+9922C>G
ENST00000553310.6:c.-4-16045C>G	ENSP00000452237.3:n.-4-16045C>G
XM_005268866.3:c.129+9922C>G	XP_005268923.1:n.129+9922C>G
XM_011538336.1:c.-5+9922C>G	XP_011536638.1:n.-5+9922C>G
XM_011538337.1:c.-5+9922C>G	XP_011536639.1:n.-5+9922C>G
XM_011538338.1:c.-5+9922C>G	XP_011536640.1:n.-5+9922C>G
NM_001320198.1:c.-5+9922C>G	NP_001307127.1:n.-5+9922C>G
XM_005268866.4:c.129+9922C>G	XP_005268923.1:n.129+9922C>G
XM_017019296.1:c.-103+9922C>G	XP_016874785.1:n.-103+9922C>G
NM_001320198.2:c.-5+9922C>G MANE Select	NP_001307127.1:n.-5+9922C>G