Canonical Allele Identifier: CA384923929
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52910529T>A (hg19) chr12:g.52516745T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516745T>A , CM000674.2:g.52516745T>A GRCh38
NC_000012.11:g.52910529T>A , CM000674.1:g.52910529T>A GRCh37
NC_000012.10:g.51196796T>A NCBI36
NG_008297.1:g.8715A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1331A>T MANE Select ENSP00000252242.4:p.Gln444Leu
ENST00000252242.8:c.1331A>T ENSP00000252242.4:p.Gln444Leu
ENST00000547890.5:n.709A>T
ENST00000548409.5:c.453A>T
ENST00000549511.5:n.538A>T
ENST00000552629.5:n.1429A>T
NM_000424.3:c.1331A>T NP_000415.2:p.Gln444Leu
NM_000424.4:c.1331A>T MANE Select NP_000415.2:p.Gln444Leu
Search 100 bp 5'
Search 100 bp 3'