Canonical Allele Identifier: CA2036418211

Gene: KRT86

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52285836_52285843delinsCTGCTCCA , CM000674.2:g.52285836_52285843delinsCTGCTCCA	GRCh38
NC_000012.11:g.52679620_52679627delinsCTGCTCCA , CM000674.1:g.52679620_52679627delinsCTGCTCCA	GRCh37
NC_000012.10:g.50965887_50965894delinsCTGCTCCA	NCBI36
NG_008184.1:g.10673_10680delinsTGGAGCAG
NG_008086.2:g.16192_16199delinsCTGCTCCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423955.7:c.-5+9890_-5+9897delinsCTGCTCCA MANE Select	ENSP00000444533.1:n.-5+9890_-5+9897delinsCTGCTCCA
ENST00000423955.6:c.-5+9890_-5+9897delinsCTGCTCCA	ENSP00000444533.1:n.-5+9890_-5+9897delinsCTGCTCCA
ENST00000553310.6:c.-4-16077_-4-16070delinsCTGCTCCA	ENSP00000452237.3:n.-4-16077_-4-16070delinsCTGCTCCA
XM_005268866.3:c.129+9890_129+9897delinsCTGCTCCA	XP_005268923.1:n.129+9890_129+9897delinsCTGCTCCA
XM_011538336.1:c.-5+9890_-5+9897delinsCTGCTCCA	XP_011536638.1:n.-5+9890_-5+9897delinsCTGCTCCA
XM_011538337.1:c.-5+9890_-5+9897delinsCTGCTCCA	XP_011536639.1:n.-5+9890_-5+9897delinsCTGCTCCA
XM_011538338.1:c.-5+9890_-5+9897delinsCTGCTCCA	XP_011536640.1:n.-5+9890_-5+9897delinsCTGCTCCA
NM_001320198.1:c.-5+9890_-5+9897delinsCTGCTCCA	NP_001307127.1:n.-5+9890_-5+9897delinsCTGCTCCA
XM_005268866.4:c.129+9890_129+9897delinsCTGCTCCA	XP_005268923.1:n.129+9890_129+9897delinsCTGCTCCA
XM_017019296.1:c.-103+9890_-103+9897delinsCTGCTCCA	XP_016874785.1:n.-103+9890_-103+9897delinsCTGCTCCA
NM_001320198.2:c.-5+9890_-5+9897delinsCTGCTCCA MANE Select	NP_001307127.1:n.-5+9890_-5+9897delinsCTGCTCCA