Canonical Allele Identifier: CA384923435
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52910435C>A (hg19) chr12:g.52516651C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516651C>A , CM000674.2:g.52516651C>A GRCh38
NC_000012.11:g.52910435C>A , CM000674.1:g.52910435C>A GRCh37
NC_000012.10:g.51196702C>A NCBI36
NG_008297.1:g.8809G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.1425G>T MANE Select ENSP00000252242.4:p.Glu475Asp
ENST00000252242.8:c.1425G>T ENSP00000252242.4:p.Glu475Asp
ENST00000548409.5:c.547G>T
ENST00000549511.5:n.632G>T
ENST00000552629.5:n.1523G>T
NM_000424.3:c.1425G>T NP_000415.2:p.Glu475Asp
NM_000424.4:c.1425G>T MANE Select NP_000415.2:p.Glu475Asp
Search 100 bp 5'
Search 100 bp 3'