Canonical Allele Identifier: CA2036540719
Gene: KRT5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520299T= , CM000674.2:g.52520299T= GRCh38
NC_000012.11:g.52914083T= , CM000674.1:g.52914083T= GRCh37
NC_000012.10:g.51200350T= NCBI36
NG_008297.1:g.5161A=

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.-3A= MANE Select ENSP00000252242.4:n.-3A=
ENST00000252242.8:c.-3A= ENSP00000252242.4:n.-3A=
ENST00000546577.1:c.-3A= ENSP00000449651.1:n.-3A=
ENST00000549420.1:c.-3A= ENSP00000447209.1:n.-3A=
ENST00000551275.1:c.-3A= ENSP00000448041.1:n.-3A=
ENST00000552629.5:n.96A=
NM_000424.3:c.-3A= NP_000415.2:n.-3A=
NM_000424.4:c.-3A= MANE Select NP_000415.2:n.-3A=