Canonical Allele Identifier: CA2036677425
Gene: KRT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52792284G= , CM000674.2:g.52792284G= GRCh38
NC_000012.11:g.53186068G= , CM000674.1:g.53186068G= GRCh37
NC_000012.10:g.51472335G= NCBI36
NG_008350.1:g.8825C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000417996.2:c.1143C= MANE Select ENSP00000413479.2:p.Ile381=
NM_057088.2:c.1143C= NP_476429.2:p.Ile381=
XM_011538324.1:c.783C= XP_011536626.1:p.Ile261=
XM_024448975.1:c.1407C= XP_024304743.1:p.Ile469=
NM_057088.3:c.1143C= MANE Select NP_476429.2:p.Ile381=