Canonical Allele Identifier: CA947707411
Gene: KRT5 HGNC NCBI

Linked Data

dbSNP Id: rs1592195725

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520313T>C , CM000674.2:g.52520313T>C GRCh38
NC_000012.11:g.52914097T>C , CM000674.1:g.52914097T>C GRCh37
NC_000012.10:g.51200364T>C NCBI36
NG_008297.1:g.5147A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.-17A>G MANE Select ENSP00000252242.4:n.-17A>G
ENST00000252242.8:c.-17A>G ENSP00000252242.4:n.-17A>G
ENST00000546577.1:c.-12-5A>G ENSP00000449651.1:n.-12-5A>G
ENST00000549420.1:c.-17A>G ENSP00000447209.1:n.-17A>G
ENST00000551275.1:c.-17A>G ENSP00000448041.1:n.-17A>G
ENST00000552629.5:n.82A>G
NM_000424.3:c.-17A>G NP_000415.2:n.-17A>G
NM_000424.4:c.-17A>G MANE Select NP_000415.2:n.-17A>G