Canonical Allele Identifier: CA2036540662
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520200T= , CM000674.2:g.52520200T= GRCh38
NC_000012.11:g.52913984T= , CM000674.1:g.52913984T= GRCh37
NC_000012.10:g.51200251T= NCBI36
NG_008297.1:g.5260A=

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.97A= MANE Select ENSP00000252242.4:p.Thr33=
ENST00000252242.8:c.97A= ENSP00000252242.4:p.Thr33=
ENST00000546577.1:c.97A= ENSP00000449651.1:p.Thr33=
ENST00000549420.1:c.43+54A= ENSP00000447209.1:n.43+54A=
ENST00000551275.1:c.97A= ENSP00000448041.1:p.Thr33=
ENST00000552629.5:n.195A=
NM_000424.3:c.97A= NP_000415.2:p.Thr33=
NM_000424.4:c.97A= MANE Select NP_000415.2:p.Thr33=