Canonical Allele Identifier: CA2036418217

Gene: KRT86

Linked Data

• dbSNP Id: rs1014535147

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52285838G>C , CM000674.2:g.52285838G>C	GRCh38
NC_000012.11:g.52679622G>C , CM000674.1:g.52679622G>C	GRCh37
NC_000012.10:g.50965889G>C	NCBI36
NG_008184.1:g.10678C>G
NG_008086.2:g.16194G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423955.7:c.-5+9892G>C MANE Select	ENSP00000444533.1:n.-5+9892G>C
ENST00000423955.6:c.-5+9892G>C	ENSP00000444533.1:n.-5+9892G>C
ENST00000553310.6:c.-4-16075G>C	ENSP00000452237.3:n.-4-16075G>C
XM_005268866.3:c.129+9892G>C	XP_005268923.1:n.129+9892G>C
XM_011538336.1:c.-5+9892G>C	XP_011536638.1:n.-5+9892G>C
XM_011538337.1:c.-5+9892G>C	XP_011536639.1:n.-5+9892G>C
XM_011538338.1:c.-5+9892G>C	XP_011536640.1:n.-5+9892G>C
NM_001320198.1:c.-5+9892G>C	NP_001307127.1:n.-5+9892G>C
XM_005268866.4:c.129+9892G>C	XP_005268923.1:n.129+9892G>C
XM_017019296.1:c.-103+9892G>C	XP_016874785.1:n.-103+9892G>C
NM_001320198.2:c.-5+9892G>C MANE Select	NP_001307127.1:n.-5+9892G>C