Canonical Allele Identifier: CA2036538739
Gene: KRT5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516324G= , CM000674.2:g.52516324G= GRCh38
NC_000012.11:g.52910108G= , CM000674.1:g.52910108G= GRCh37
NC_000012.10:g.51196375G= NCBI36
NG_008297.1:g.9136C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1439+313C= MANE Select ENSP00000252242.4:n.1439+313C=
ENST00000252242.8:c.1439+313C= ENSP00000252242.4:n.1439+313C=
ENST00000548409.5:c.561+313C=
ENST00000549511.5:n.646+313C=
ENST00000552629.5:n.1850C=
NM_000424.3:c.1439+313C= NP_000415.2:n.1439+313C=
NM_000424.4:c.1439+313C= MANE Select NP_000415.2:n.1439+313C=
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