Canonical Allele Identifier: CA384929100
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52913615G>A (hg19) chr12:g.52519831G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519831G>A , CM000674.2:g.52519831G>A GRCh38
NC_000012.11:g.52913615G>A , CM000674.1:g.52913615G>A GRCh37
NC_000012.10:g.51199882G>A NCBI36
NG_008297.1:g.5629C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.466C>T MANE Select ENSP00000252242.4:p.Gln156Ter
ENST00000252242.8:c.466C>T ENSP00000252242.4:p.Gln156Ter
ENST00000549420.1:c.136C>T ENSP00000447209.1:p.Gln46Ter
ENST00000551275.1:c.361C>T ENSP00000448041.1:p.Gln121Ter
ENST00000552629.5:n.564C>T
NM_000424.3:c.466C>T NP_000415.2:p.Gln156Ter
NM_000424.4:c.466C>T MANE Select NP_000415.2:p.Gln156Ter
Search 100 bp 5'
Search 100 bp 3'