Canonical Allele Identifier: CA2036538975
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516766T= , CM000674.2:g.52516766T= GRCh38
NC_000012.11:g.52910550T= , CM000674.1:g.52910550T= GRCh37
NC_000012.10:g.51196817T= NCBI36
NG_008297.1:g.8694A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1310A= MANE Select ENSP00000252242.4:p.Glu437=
ENST00000252242.8:c.1310A= ENSP00000252242.4:p.Glu437=
ENST00000547890.5:n.688A=
ENST00000548409.5:c.432A=
ENST00000549511.5:n.517A=
ENST00000552629.5:n.1408A=
NM_000424.3:c.1310A= NP_000415.2:p.Glu437=
NM_000424.4:c.1310A= MANE Select NP_000415.2:p.Glu437=