Canonical Allele Identifier: CA772039817
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1209320972

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584409_41584414del , CM000679.2:g.41584409_41584414del GRCh38
NC_000017.10:g.39740661_39740666del , CM000679.1:g.39740661_39740666del GRCh37
NC_000017.9:g.36994187_36994192del NCBI36
NG_008624.1:g.7482_7487del

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.609-1_613del
ENST00000167586.6:c.609-1_613del
ENST00000476662.1:n.58_63del
NM_000526.4:c.609-1_613del
NM_000526.5:c.609-1_613del