Canonical Allele Identifier: CA384959989
Gene: KRT1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.53069256A>C (hg19) chr12:g.52675472A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52675472A>C , CM000674.2:g.52675472A>C GRCh38
NC_000012.11:g.53069256A>C , CM000674.1:g.53069256A>C GRCh37
NC_000012.10:g.51355523A>C NCBI36
NG_008364.1:g.9936T>G
NG_008364.2:g.9936T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252244.3:c.1656T>G MANE Select ENSP00000252244.3:p.Tyr552Ter
NM_006121.3:c.1656T>G NP_006112.3:p.Tyr552Ter
NM_006121.4:c.1656T>G MANE Select NP_006112.3:p.Tyr552Ter
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