Canonical Allele Identifier: CA384928740
Gene: KRT5 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519750T>G , CM000674.2:g.52519750T>G GRCh38
NC_000012.11:g.52913534T>G , CM000674.1:g.52913534T>G GRCh37
NC_000012.10:g.51199801T>G NCBI36
NG_008297.1:g.5710A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.547A>C MANE Select ENSP00000252242.4:p.Ile183Leu
ENST00000252242.8:c.547A>C ENSP00000252242.4:p.Ile183Leu
ENST00000549420.1:c.217A>C ENSP00000447209.1:p.Ile73Leu
ENST00000552629.5:n.645A>C
NM_000424.3:c.547A>C NP_000415.2:p.Ile183Leu
NM_000424.4:c.547A>C MANE Select NP_000415.2:p.Ile183Leu