Canonical Allele Identifier: CA2618932935
Gene: KRT5 HGNC NCBI

Linked Data

gnomAD v4: 12-52520174-G-GCCACCC
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520177_52520182dup , CM000674.2:g.52520177_52520182dup GRCh38
NC_000012.11:g.52913961_52913966dup , CM000674.1:g.52913961_52913966dup GRCh37
NC_000012.10:g.51200228_51200233dup NCBI36
NG_008297.1:g.5280_5285dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.117_122dup MANE Select ENSP00000252242.4:p.Gly41_Gly42insGlyGly
ENST00000252242.8:c.117_122dup ENSP00000252242.4:p.Gly41_Gly42insGlyGly
ENST00000546577.1:c.117_122dup ENSP00000449651.1:p.Gly41_Gly42insGlyGly
ENST00000549420.1:c.43+74_43+79dup ENSP00000447209.1:n.43+74_43+79dup
ENST00000551275.1:c.117_122dup ENSP00000448041.1:p.Gly41_Gly42insGlyGly
ENST00000552629.5:n.215_220dup
NM_000424.3:c.117_122dup NP_000415.2:p.Gly41_Gly42insGlyGly
NM_000424.4:c.117_122dup MANE Select NP_000415.2:p.Gly41_Gly42insGlyGly
Search 100 bp 5'
Search 100 bp 3'