Canonical Allele Identifier: CA2618932590
Gene: KRT5 HGNC NCBI

Linked Data

gnomAD v4: 12-52519669-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519669A>C , CM000674.2:g.52519669A>C GRCh38
NC_000012.11:g.52913453A>C , CM000674.1:g.52913453A>C GRCh37
NC_000012.10:g.51199720A>C NCBI36
NG_008297.1:g.5791T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.555+73T>G MANE Select ENSP00000252242.4:n.555+73T>G
ENST00000252242.8:c.555+73T>G ENSP00000252242.4:n.555+73T>G
ENST00000549420.1:c.225+73T>G ENSP00000447209.1:n.225+73T>G
ENST00000552629.5:n.653+73T>G
NM_000424.3:c.555+73T>G NP_000415.2:n.555+73T>G
NM_000424.4:c.555+73T>G MANE Select NP_000415.2:n.555+73T>G
Search 100 bp 5'
Search 100 bp 3'