Canonical Allele Identifier: CA2036677367
Gene: KRT3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52792247G= , CM000674.2:g.52792247G= GRCh38
NC_000012.11:g.53186031G= , CM000674.1:g.53186031G= GRCh37
NC_000012.10:g.51472298G= NCBI36
NG_008350.1:g.8862C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000417996.2:c.1180C= MANE Select ENSP00000413479.2:p.Gln394=
NM_057088.2:c.1180C= NP_476429.2:p.Gln394=
XM_011538324.1:c.820C= XP_011536626.1:p.Gln274=
XM_024448975.1:c.1444C= XP_024304743.1:p.Gln482=
NM_057088.3:c.1180C= MANE Select NP_476429.2:p.Gln394=