Canonical Allele Identifier: CA2036540379
Gene: KRT5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519643T= , CM000674.2:g.52519643T= GRCh38
NC_000012.11:g.52913427T= , CM000674.1:g.52913427T= GRCh37
NC_000012.10:g.51199694T= NCBI36
NG_008297.1:g.5817A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.555+99A= MANE Select ENSP00000252242.4:n.555+99A=
ENST00000252242.8:c.555+99A= ENSP00000252242.4:n.555+99A=
ENST00000549420.1:c.225+99A= ENSP00000447209.1:n.225+99A=
ENST00000552629.5:n.653+99A=
NM_000424.3:c.555+99A= NP_000415.2:n.555+99A=
NM_000424.4:c.555+99A= MANE Select NP_000415.2:n.555+99A=
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