Canonical Allele Identifier: CA384988670
Gene: KRT4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.53203237T>C (hg19) chr12:g.52809453T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52809453T>C , CM000674.2:g.52809453T>C GRCh38
NC_000012.11:g.53203237T>C , CM000674.1:g.53203237T>C GRCh37
NC_000012.10:g.51489504T>C NCBI36
NG_007380.1:g.10099A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.764A>G MANE Select ENSP00000448220.1:p.Lys255Arg
ENST00000548097.5:c.*276A>G ENSP00000449755.1:n.*276A>G
ENST00000549295.1:n.198A>G
ENST00000551956.1:c.764A>G ENSP00000448220.1:p.Lys255Arg
ENST00000552668.1:c.*169A>G ENSP00000447320.1:n.*169A>G
NM_002272.3:c.764A>G NP_002263.3:p.Lys255Arg
NM_002272.4:c.764A>G MANE Select NP_002263.3:p.Lys255Arg
Search 100 bp 5'
Search 100 bp 3'