Canonical Allele Identifier: CA3250141982
Community Standard Title: NM_000424.4(KRT5):c.591_594delinsAACA (p.Asp197Glu)
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519122_52519125delinsTGTT , CM000674.2:g.52519122_52519125delinsTGTT GRCh38
NC_000012.11:g.52912906_52912909delinsTGTT , CM000674.1:g.52912906_52912909delinsTGTT GRCh37
NC_000012.10:g.51199173_51199176delinsTGTT NCBI36
NG_008297.1:g.6335_6338delinsAACA

Transcript Alleles

HGVS Amino-acid Change
NM_000424.4:c.591_594delinsAACA MANE Select NP_000415.2:p.Asp197Glu
ENST00000252242.9:c.591_594delinsAACA MANE Select ENSP00000252242.4:p.Asp197Glu
NM_000424.3:c.591_594delinsAACA NP_000415.2:p.Asp197Glu
ENST00000252242.8:c.591_594delinsAACA ENSP00000252242.4:p.Asp197Glu
ENST00000549420.1:c.261_264delinsAACA ENSP00000447209.1:p.Asp87Glu
ENST00000551013.1:n.119_122delinsAACA
ENST00000552629.5:n.689_692delinsAACA