Canonical Allele Identifier: CA384962376
Gene: KRT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.53070120T>C (hg19) chr12:g.52676336T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52676336T>C , CM000674.2:g.52676336T>C GRCh38
NC_000012.11:g.53070120T>C , CM000674.1:g.53070120T>C GRCh37
NC_000012.10:g.51356387T>C NCBI36
NG_008364.1:g.9072A>G
NG_008364.2:g.9072A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000252244.3:c.1414A>G MANE Select ENSP00000252244.3:p.Lys472Glu
ENST00000548765.1:n.488A>G
NM_006121.3:c.1414A>G NP_006112.3:p.Lys472Glu
NM_006121.4:c.1414A>G MANE Select NP_006112.3:p.Lys472Glu
Search 100 bp 5'
Search 100 bp 3'