Canonical Allele Identifier: CA2618932976
Gene: KRT5 HGNC NCBI

Linked Data

gnomAD v4: 12-52520357-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520357A>G , CM000674.2:g.52520357A>G GRCh38
NC_000012.11:g.52914141A>G , CM000674.1:g.52914141A>G GRCh37
NC_000012.10:g.51200408A>G NCBI36
NG_008297.1:g.5103T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.-61T>C MANE Select ENSP00000252242.4:n.-61T>C
ENST00000252242.8:c.-61T>C ENSP00000252242.4:n.-61T>C
ENST00000546577.1:c.-13+40T>C ENSP00000449651.1:n.-13+40T>C
ENST00000549420.1:c.-61T>C ENSP00000447209.1:n.-61T>C
ENST00000551275.1:c.-61T>C ENSP00000448041.1:n.-61T>C
ENST00000552629.5:n.38T>C
NM_000424.3:c.-61T>C NP_000415.2:n.-61T>C
NM_000424.4:c.-61T>C MANE Select NP_000415.2:n.-61T>C
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