Canonical Allele Identifier: CA2036540483
Gene: KRT5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519853_52519855delinsACT , CM000674.2:g.52519853_52519855delinsACT GRCh38
NC_000012.11:g.52913637_52913639delinsACT , CM000674.1:g.52913637_52913639delinsACT GRCh37
NC_000012.10:g.51199904_51199906delinsACT NCBI36
NG_008297.1:g.5605_5607delinsAGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.442_444delinsAGT MANE Select ENSP00000252242.4:p.Ser148=
ENST00000252242.8:c.442_444delinsAGT ENSP00000252242.4:p.Ser148=
ENST00000549420.1:c.112_114delinsAGT ENSP00000447209.1:p.Ser38=
ENST00000551275.1:c.337_339delinsAGT ENSP00000448041.1:p.Ser113=
ENST00000552629.5:n.540_542delinsAGT
NM_000424.3:c.442_444delinsAGT NP_000415.2:p.Ser148=
NM_000424.4:c.442_444delinsAGT MANE Select NP_000415.2:p.Ser148=
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