Canonical Allele Identifier: CA2556190766

Gene: KRT5

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.52520182_52520183insAT , CM000674.2:g.52520182_52520183insAT	GRCh38
NC_000012.11:g.52913966_52913967insAT , CM000674.1:g.52913966_52913967insAT	GRCh37
NC_000012.10:g.51200233_51200234insAT	NCBI36
NG_008297.1:g.5277_5278insAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000252242.9:c.114_115insAT MANE Select	ENSP00000252242.4:p.Gly39MetfsTer?
ENST00000252242.8:c.114_115insAT	ENSP00000252242.4:p.Gly39MetfsTer?
ENST00000546577.1:c.114_115insAT	ENSP00000449651.1:p.Gly39MetfsTer?
ENST00000549420.1:c.43+71_43+72insAT	ENSP00000447209.1:n.43+71_43+72insAT
ENST00000551275.1:c.114_115insAT	ENSP00000448041.1:p.Gly39MetfsTer?
ENST00000552629.5:n.212_213insAT
NM_000424.3:c.114_115insAT	NP_000415.2:p.Gly39MetfsTer?
NM_000424.4:c.114_115insAT MANE Select	NP_000415.2:p.Gly39MetfsTer?