Canonical Allele Identifier: CA384989047
Gene: KRT4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.53205589T>A (hg19) chr12:g.52811805T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52811805T>A , CM000674.2:g.52811805T>A GRCh38
NC_000012.11:g.53205589T>A , CM000674.1:g.53205589T>A GRCh37
NC_000012.10:g.51491856T>A NCBI36
NG_007380.1:g.7747A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000551956.2:c.635A>T MANE Select ENSP00000448220.1:p.Glu212Val
ENST00000548097.5:c.*147A>T ENSP00000449755.1:n.*147A>T
ENST00000551436.1:n.193A>T
ENST00000551956.1:c.635A>T ENSP00000448220.1:p.Glu212Val
ENST00000552668.1:c.*83-989A>T ENSP00000447320.1:n.*83-989A>T
NM_002272.3:c.635A>T NP_002263.3:p.Glu212Val
NM_002272.4:c.635A>T MANE Select NP_002263.3:p.Glu212Val
Search 100 bp 5'
Search 100 bp 3'