Canonical Allele Identifier: CA2036619200
Gene: KRT1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52675532A= , CM000674.2:g.52675532A= GRCh38
NC_000012.11:g.53069316A= , CM000674.1:g.53069316A= GRCh37
NC_000012.10:g.51355583A= NCBI36
NG_008364.1:g.9876T=
NG_008364.2:g.9876T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252244.3:c.1596T= MANE Select ENSP00000252244.3:p.Tyr532=
NM_006121.3:c.1596T= NP_006112.3:p.Tyr532=
NM_006121.4:c.1596T= MANE Select NP_006112.3:p.Tyr532=
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