Canonical Allele Identifier: CA2036538977
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516769T= , CM000674.2:g.52516769T= GRCh38
NC_000012.11:g.52910553T= , CM000674.1:g.52910553T= GRCh37
NC_000012.10:g.51196820T= NCBI36
NG_008297.1:g.8691A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1307A= MANE Select ENSP00000252242.4:p.Glu436=
ENST00000252242.8:c.1307A= ENSP00000252242.4:p.Glu436=
ENST00000547890.5:n.685A=
ENST00000548409.5:c.429A=
ENST00000549511.5:n.514A=
ENST00000552629.5:n.1405A=
NM_000424.3:c.1307A= NP_000415.2:p.Glu436=
NM_000424.4:c.1307A= MANE Select NP_000415.2:p.Glu436=