Canonical Allele Identifier: CA2036538927
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516666G= , CM000674.2:g.52516666G= GRCh38
NC_000012.11:g.52910450G= , CM000674.1:g.52910450G= GRCh37
NC_000012.10:g.51196717G= NCBI36
NG_008297.1:g.8794C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1410C= MANE Select ENSP00000252242.4:p.Tyr470=
ENST00000252242.8:c.1410C= ENSP00000252242.4:p.Tyr470=
ENST00000548409.5:c.532C=
ENST00000549511.5:n.617C=
ENST00000552629.5:n.1508C=
NM_000424.3:c.1410C= NP_000415.2:p.Tyr470=
NM_000424.4:c.1410C= MANE Select NP_000415.2:p.Tyr470=