Canonical Allele Identifier: CA384957043
Gene: KRT1 HGNC NCBI
MyVariant.info:
Revel Score:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52675230T>A , CM000674.2:g.52675230T>A GRCh38
NC_000012.11:g.53069014T>A , CM000674.1:g.53069014T>A GRCh37
NC_000012.10:g.51355281T>A NCBI36
NG_008364.1:g.10178A>T
NG_008364.2:g.10178A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252244.3:c.1898A>T MANE Select ENSP00000252244.3:p.Lys633Met
NM_006121.3:c.1898A>T NP_006112.3:p.Lys633Met
NM_006121.4:c.1898A>T MANE Select NP_006112.3:p.Lys633Met