Canonical Allele Identifier: CA2036418290

Gene: KRT86

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52285909_52285910delinsCA , CM000674.2:g.52285909_52285910delinsCA	GRCh38
NC_000012.11:g.52679693_52679694delinsCA , CM000674.1:g.52679693_52679694delinsCA	GRCh37
NC_000012.10:g.50965960_50965961delinsCA	NCBI36
NG_008184.1:g.10606_10607delinsTG
NG_008086.2:g.16265_16266delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423955.7:c.-5+9963_-5+9964delinsCA MANE Select	ENSP00000444533.1:n.-5+9963_-5+9964delinsCA
ENST00000423955.6:c.-5+9963_-5+9964delinsCA	ENSP00000444533.1:n.-5+9963_-5+9964delinsCA
ENST00000553310.6:c.-4-16004_-4-16003delinsCA	ENSP00000452237.3:n.-4-16004_-4-16003delinsCA
XM_005268866.3:c.129+9963_129+9964delinsCA	XP_005268923.1:n.129+9963_129+9964delinsCA
XM_011538336.1:c.-5+9963_-5+9964delinsCA	XP_011536638.1:n.-5+9963_-5+9964delinsCA
XM_011538337.1:c.-5+9963_-5+9964delinsCA	XP_011536639.1:n.-5+9963_-5+9964delinsCA
XM_011538338.1:c.-5+9963_-5+9964delinsCA	XP_011536640.1:n.-5+9963_-5+9964delinsCA
NM_001320198.1:c.-5+9963_-5+9964delinsCA	NP_001307127.1:n.-5+9963_-5+9964delinsCA
XM_005268866.4:c.129+9963_129+9964delinsCA	XP_005268923.1:n.129+9963_129+9964delinsCA
XM_017019296.1:c.-103+9963_-103+9964delinsCA	XP_016874785.1:n.-103+9963_-103+9964delinsCA
NM_001320198.2:c.-5+9963_-5+9964delinsCA MANE Select	NP_001307127.1:n.-5+9963_-5+9964delinsCA