Canonical Allele Identifier: CA2036540491
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519870C= , CM000674.2:g.52519870C= GRCh38
NC_000012.11:g.52913654C= , CM000674.1:g.52913654C= GRCh37
NC_000012.10:g.51199921C= NCBI36
NG_008297.1:g.5590G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.427G= MANE Select ENSP00000252242.4:p.Val143=
ENST00000252242.8:c.427G= ENSP00000252242.4:p.Val143=
ENST00000549420.1:c.97G= ENSP00000447209.1:p.Val33=
ENST00000551275.1:c.322G= ENSP00000448041.1:p.Val108=
ENST00000552629.5:n.525G=
NM_000424.3:c.427G= NP_000415.2:p.Val143=
NM_000424.4:c.427G= MANE Select NP_000415.2:p.Val143=