Canonical Allele Identifier: CA2036540388
Gene: KRT5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519675C= , CM000674.2:g.52519675C= GRCh38
NC_000012.11:g.52913459C= , CM000674.1:g.52913459C= GRCh37
NC_000012.10:g.51199726C= NCBI36
NG_008297.1:g.5785G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.555+67G= MANE Select ENSP00000252242.4:n.555+67G=
ENST00000252242.8:c.555+67G= ENSP00000252242.4:n.555+67G=
ENST00000549420.1:c.225+67G= ENSP00000447209.1:n.225+67G=
ENST00000552629.5:n.653+67G=
NM_000424.3:c.555+67G= NP_000415.2:n.555+67G=
NM_000424.4:c.555+67G= MANE Select NP_000415.2:n.555+67G=
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