Canonical Allele Identifier: CA480076210
Gene: KRT4 HGNC NCBI

Linked Data

gnomAD v4: 12-52813996-A-G
MyVariant Identifiers: chr12:g.53207780A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52813996A>G , CM000674.2:g.52813996A>G GRCh38
NC_000012.11:g.53207780A>G , CM000674.1:g.53207780A>G GRCh37
NC_000012.10:g.51494047A>G NCBI36
NG_007380.1:g.5556T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.63T>C MANE Select ENSP00000448220.1:p.Ile21=
ENST00000548097.5:c.63T>C ENSP00000449755.1:p.Ile21=
ENST00000551956.1:c.63T>C ENSP00000448220.1:p.Ile21=
ENST00000552668.1:c.63T>C ENSP00000447320.1:p.Ile21=
NM_002272.3:c.63T>C NP_002263.3:p.Ile21=
NM_002272.4:c.63T>C MANE Select NP_002263.3:p.Ile21=
Search 100 bp 5'
Search 100 bp 3'