Canonical Allele Identifier: CA2036418183

Gene: KRT86

Linked Data

• dbSNP Id: rs1937909354

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52285814_52285823del , CM000674.2:g.52285814_52285823del	GRCh38
NC_000012.11:g.52679598_52679607del , CM000674.1:g.52679598_52679607del	GRCh37
NC_000012.10:g.50965865_50965874del	NCBI36
NG_008184.1:g.10696_10705del
NG_008086.2:g.16170_16179del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000423955.7:c.-5+9868_-5+9877del MANE Select	ENSP00000444533.1:n.-5+9868_-5+9877del
ENST00000423955.6:c.-5+9868_-5+9877del	ENSP00000444533.1:n.-5+9868_-5+9877del
ENST00000553310.6:c.-4-16099_-4-16090del	ENSP00000452237.3:n.-4-16099_-4-16090del
XM_005268866.3:c.129+9868_129+9877del	XP_005268923.1:n.129+9868_129+9877del
XM_011538336.1:c.-5+9868_-5+9877del	XP_011536638.1:n.-5+9868_-5+9877del
XM_011538337.1:c.-5+9868_-5+9877del	XP_011536639.1:n.-5+9868_-5+9877del
XM_011538338.1:c.-5+9868_-5+9877del	XP_011536640.1:n.-5+9868_-5+9877del
NM_001320198.1:c.-5+9868_-5+9877del	NP_001307127.1:n.-5+9868_-5+9877del
XM_005268866.4:c.129+9868_129+9877del	XP_005268923.1:n.129+9868_129+9877del
XM_017019296.1:c.-103+9868_-103+9877del	XP_016874785.1:n.-103+9868_-103+9877del
NM_001320198.2:c.-5+9868_-5+9877del MANE Select	NP_001307127.1:n.-5+9868_-5+9877del