Canonical Allele Identifier: CA2618967542
Gene: KRT4 HGNC NCBI

Linked Data

gnomAD v4: 12-52813943-GC-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52813944del , CM000674.2:g.52813944del GRCh38
NC_000012.11:g.53207728del , CM000674.1:g.53207728del GRCh37
NC_000012.10:g.51493995del NCBI36
NG_007380.1:g.5608del

Transcript Alleles

HGVS Amino-acid change
ENST00000551956.2:c.115del MANE Select ENSP00000448220.1:p.Ala39LeufsTer25
ENST00000548097.5:c.115del ENSP00000449755.1:p.Ala39LeufsTer25
ENST00000551956.1:c.115del ENSP00000448220.1:p.Ala39LeufsTer25
ENST00000552668.1:c.115del ENSP00000447320.1:p.Ala39LeufsTer25
NM_002272.3:c.115del NP_002263.3:p.Ala39LeufsTer25
NM_002272.4:c.115del MANE Select NP_002263.3:p.Ala39LeufsTer25
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Search 100 bp 3'