Canonical Allele Identifier: CA2618932992
Gene: KRT5 HGNC NCBI

Linked Data

gnomAD v4: 12-52520380-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520380G>T , CM000674.2:g.52520380G>T GRCh38
NC_000012.11:g.52914164G>T , CM000674.1:g.52914164G>T GRCh37
NC_000012.10:g.51200431G>T NCBI36
NG_008297.1:g.5080C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.-84C>A MANE Select ENSP00000252242.4:n.-84C>A
ENST00000252242.8:c.-84C>A ENSP00000252242.4:n.-84C>A
ENST00000546577.1:c.-13+17C>A ENSP00000449651.1:n.-13+17C>A
ENST00000551275.1:c.-84C>A ENSP00000448041.1:n.-84C>A
ENST00000552629.5:n.15C>A
NM_000424.3:c.-84C>A NP_000415.2:n.-84C>A
NM_000424.4:c.-84C>A MANE Select NP_000415.2:n.-84C>A
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