Canonical Allele Identifier: CA2036538763
Gene: KRT5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516386G= , CM000674.2:g.52516386G= GRCh38
NC_000012.11:g.52910170G= , CM000674.1:g.52910170G= GRCh37
NC_000012.10:g.51196437G= NCBI36
NG_008297.1:g.9074C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1439+251C= MANE Select ENSP00000252242.4:n.1439+251C=
ENST00000252242.8:c.1439+251C= ENSP00000252242.4:n.1439+251C=
ENST00000548409.5:c.561+251C=
ENST00000549511.5:n.646+251C=
ENST00000552629.5:n.1788C=
NM_000424.3:c.1439+251C= NP_000415.2:n.1439+251C=
NM_000424.4:c.1439+251C= MANE Select NP_000415.2:n.1439+251C=
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