Canonical Allele Identifier: CA2036538916
Gene: KRT5 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516648G= , CM000674.2:g.52516648G= GRCh38
NC_000012.11:g.52910432G= , CM000674.1:g.52910432G= GRCh37
NC_000012.10:g.51196699G= NCBI36
NG_008297.1:g.8812C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1428C= MANE Select ENSP00000252242.4:p.Gly476=
ENST00000252242.8:c.1428C= ENSP00000252242.4:p.Gly476=
ENST00000548409.5:c.550C=
ENST00000549511.5:n.635C=
ENST00000552629.5:n.1526C=
NM_000424.3:c.1428C= NP_000415.2:p.Gly476=
NM_000424.4:c.1428C= MANE Select NP_000415.2:p.Gly476=
Search 100 bp 5'
Search 100 bp 3'