Canonical Allele Identifier: CA384985795
Gene: KRT4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.53201476T>G (hg19) chr12:g.52807692T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52807692T>G , CM000674.2:g.52807692T>G GRCh38
NC_000012.11:g.53201476T>G , CM000674.1:g.53201476T>G GRCh37
NC_000012.10:g.51487743T>G NCBI36
NG_007380.1:g.11860A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.1298A>C MANE Select ENSP00000448220.1:p.Asp433Ala
ENST00000548097.5:c.*810A>C ENSP00000449755.1:n.*810A>C
ENST00000551956.1:c.1298A>C ENSP00000448220.1:p.Asp433Ala
NM_002272.3:c.1298A>C NP_002263.3:p.Asp433Ala
NM_002272.4:c.1298A>C MANE Select NP_002263.3:p.Asp433Ala
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