Canonical Allele Identifier: CA480070510
Gene: KRT5 HGNC NCBI

Linked Data

gnomAD v4: 12-52519991-A-T
MyVariant Identifiers: chr12:g.52913775A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519991A>T , CM000674.2:g.52519991A>T GRCh38
NC_000012.11:g.52913775A>T , CM000674.1:g.52913775A>T GRCh37
NC_000012.10:g.51200042A>T NCBI36
NG_008297.1:g.5469T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.306T>A MANE Select ENSP00000252242.4:p.Gly102=
ENST00000252242.8:c.306T>A ENSP00000252242.4:p.Gly102=
ENST00000546577.1:c.306T>A ENSP00000449651.1:p.Gly102=
ENST00000549420.1:c.44-68T>A ENSP00000447209.1:n.44-68T>A
ENST00000551275.1:c.201T>A ENSP00000448041.1:p.Gly67=
ENST00000552629.5:n.404T>A
NM_000424.3:c.306T>A NP_000415.2:p.Gly102=
NM_000424.4:c.306T>A MANE Select NP_000415.2:p.Gly102=
Search 100 bp 5'
Search 100 bp 3'