Canonical Allele Identifier: CA6582968
Gene: KRT5 HGNC NCBI

Linked Data

dbSNP Id: rs762155109

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520306T>A , CM000674.2:g.52520306T>A GRCh38
NC_000012.11:g.52914090T>A , CM000674.1:g.52914090T>A GRCh37
NC_000012.10:g.51200357T>A NCBI36
NG_008297.1:g.5154A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000252242.9:c.-10A>T MANE Select ENSP00000252242.4:n.-10A>T
ENST00000252242.8:c.-10A>T ENSP00000252242.4:n.-10A>T
ENST00000546577.1:c.-10A>T ENSP00000449651.1:n.-10A>T
ENST00000549420.1:c.-10A>T ENSP00000447209.1:n.-10A>T
ENST00000551275.1:c.-10A>T ENSP00000448041.1:n.-10A>T
ENST00000552629.5:n.89A>T
NM_000424.3:c.-10A>T NP_000415.2:n.-10A>T
NM_000424.4:c.-10A>T MANE Select NP_000415.2:n.-10A>T