Canonical Allele Identifier: CA645583462
Gene: KRT4 HGNC NCBI

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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814096A>G , CM000674.2:g.52814096A>G GRCh38
NC_000012.11:g.53207880A>G , CM000674.1:g.53207880A>G GRCh37
NC_000012.10:g.51494147A>G NCBI36
NG_007380.1:g.5456T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.-38T>C MANE Select ENSP00000448220.1:n.-38T>C
ENST00000548097.5:c.-38T>C ENSP00000449755.1:n.-38T>C
ENST00000551956.1:c.-38T>C ENSP00000448220.1:n.-38T>C
ENST00000552668.1:c.-38T>C ENSP00000447320.1:n.-38T>C
NM_002272.3:c.-38T>C NP_002263.3:n.-38T>C
NM_002272.4:c.-38T>C MANE Select NP_002263.3:n.-38T>C
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