Canonical Allele Identifier: CA2618932982
Gene: KRT5 HGNC NCBI

Linked Data

gnomAD v4: 12-52520363-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520363G>C , CM000674.2:g.52520363G>C GRCh38
NC_000012.11:g.52914147G>C , CM000674.1:g.52914147G>C GRCh37
NC_000012.10:g.51200414G>C NCBI36
NG_008297.1:g.5097C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.-67C>G MANE Select ENSP00000252242.4:n.-67C>G
ENST00000252242.8:c.-67C>G ENSP00000252242.4:n.-67C>G
ENST00000546577.1:c.-13+34C>G ENSP00000449651.1:n.-13+34C>G
ENST00000549420.1:c.-67C>G ENSP00000447209.1:n.-67C>G
ENST00000551275.1:c.-67C>G ENSP00000448041.1:n.-67C>G
ENST00000552629.5:n.32C>G
NM_000424.3:c.-67C>G NP_000415.2:n.-67C>G
NM_000424.4:c.-67C>G MANE Select NP_000415.2:n.-67C>G
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