Canonical Allele Identifier: CA2036598644
Gene: KRT2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652113_52652114delinsTC , CM000674.2:g.52652113_52652114delinsTC GRCh38
NC_000012.11:g.53045897_53045898delinsTC , CM000674.1:g.53045897_53045898delinsTC GRCh37
NC_000012.10:g.51332164_51332165delinsTC NCBI36
NG_008296.1:g.5062_5063delinsGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.29_30delinsGA MANE Select ENSP00000310861.3:p.Arg10=
ENST00000309680.3:c.29_30delinsGA ENSP00000310861.3:p.Arg10=
NM_000423.2:c.29_30delinsGA NP_000414.2:p.Arg10=
NM_000423.3:c.29_30delinsGA MANE Select NP_000414.2:p.Arg10=
Search 100 bp 5'
Search 100 bp 3'