Canonical Allele Identifier: CA2036619581
Gene: KRT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52676334C= , CM000674.2:g.52676334C= GRCh38
NC_000012.11:g.53070118C= , CM000674.1:g.53070118C= GRCh37
NC_000012.10:g.51356385C= NCBI36
NG_008364.1:g.9074G=
NG_008364.2:g.9074G=

Transcript Alleles

HGVS Amino-acid change
ENST00000252244.3:c.1416G= MANE Select ENSP00000252244.3:p.Lys472=
ENST00000548765.1:n.490G=
NM_006121.3:c.1416G= NP_006112.3:p.Lys472=
NM_006121.4:c.1416G= MANE Select NP_006112.3:p.Lys472=