Canonical Allele Identifier: CA2036538846
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516541A= , CM000674.2:g.52516541A= GRCh38
NC_000012.11:g.52910325A= , CM000674.1:g.52910325A= GRCh37
NC_000012.10:g.51196592A= NCBI36
NG_008297.1:g.8919T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1439+96T= MANE Select ENSP00000252242.4:n.1439+96T=
ENST00000252242.8:c.1439+96T= ENSP00000252242.4:n.1439+96T=
ENST00000548409.5:c.561+96T=
ENST00000549511.5:n.646+96T=
ENST00000552629.5:n.1633T=
NM_000424.3:c.1439+96T= NP_000415.2:n.1439+96T=
NM_000424.4:c.1439+96T= MANE Select NP_000415.2:n.1439+96T=