Canonical Allele Identifier: CA2036619082
Gene: KRT1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52675374C= , CM000674.2:g.52675374C= GRCh38
NC_000012.11:g.53069158C= , CM000674.1:g.53069158C= GRCh37
NC_000012.10:g.51355425C= NCBI36
NG_008364.1:g.10034G=
NG_008364.2:g.10034G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252244.3:c.1754G= MANE Select ENSP00000252244.3:p.Gly585=
NM_006121.3:c.1754G= NP_006112.3:p.Gly585=
NM_006121.4:c.1754G= MANE Select NP_006112.3:p.Gly585=
Search 100 bp 5'
Search 100 bp 3'