Canonical Allele Identifier: CA2036598623
Gene: KRT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652095_52652096delinsTC , CM000674.2:g.52652095_52652096delinsTC GRCh38
NC_000012.11:g.53045879_53045880delinsTC , CM000674.1:g.53045879_53045880delinsTC GRCh37
NC_000012.10:g.51332146_51332147delinsTC NCBI36
NG_008296.1:g.5080_5081delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.47_48delinsGA MANE Select ENSP00000310861.3:p.Gly16=
ENST00000309680.3:c.47_48delinsGA ENSP00000310861.3:p.Gly16=
NM_000423.2:c.47_48delinsGA NP_000414.2:p.Gly16=
NM_000423.3:c.47_48delinsGA MANE Select NP_000414.2:p.Gly16=
Search 100 bp 5'
Search 100 bp 3'