Canonical Allele Identifier: CA2036598557
Gene: KRT2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52652038_52652041delinsTCTC , CM000674.2:g.52652038_52652041delinsTCTC GRCh38
NC_000012.11:g.53045822_53045825delinsTCTC , CM000674.1:g.53045822_53045825delinsTCTC GRCh37
NC_000012.10:g.51332089_51332092delinsTCTC NCBI36
NG_008296.1:g.5135_5138delinsGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000309680.4:c.102_105delinsGAGA MANE Select ENSP00000310861.3:p.Arg34=
ENST00000309680.3:c.102_105delinsGAGA ENSP00000310861.3:p.Arg34=
NM_000423.2:c.102_105delinsGAGA NP_000414.2:p.Arg34=
NM_000423.3:c.102_105delinsGAGA MANE Select NP_000414.2:p.Arg34=