Canonical Allele Identifier: CA2618932949
Gene: KRT5 HGNC NCBI

Linked Data

gnomAD v4: 12-52520318-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520318C>T , CM000674.2:g.52520318C>T GRCh38
NC_000012.11:g.52914102C>T , CM000674.1:g.52914102C>T GRCh37
NC_000012.10:g.51200369C>T NCBI36
NG_008297.1:g.5142G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.-22G>A MANE Select ENSP00000252242.4:n.-22G>A
ENST00000252242.8:c.-22G>A ENSP00000252242.4:n.-22G>A
ENST00000546577.1:c.-12-10G>A ENSP00000449651.1:n.-12-10G>A
ENST00000549420.1:c.-22G>A ENSP00000447209.1:n.-22G>A
ENST00000551275.1:c.-22G>A ENSP00000448041.1:n.-22G>A
ENST00000552629.5:n.77G>A
NM_000424.3:c.-22G>A NP_000415.2:n.-22G>A
NM_000424.4:c.-22G>A MANE Select NP_000415.2:n.-22G>A
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