Canonical Allele Identifier: CA2733826767

Gene: KRT14

Linked Data

• dbSNP Id: rs2144583485

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584065_41584072del , CM000679.2:g.41584065_41584072del	GRCh38
NC_000017.10:g.39740317_39740324del , CM000679.1:g.39740317_39740324del	GRCh37
NC_000017.9:g.36993843_36993850del	NCBI36
NG_008624.1:g.7825_7832del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-150_766-143del MANE Select	ENSP00000167586.6:n.766-150_766-143del
ENST00000167586.6:c.766-150_766-143del	ENSP00000167586.6:n.766-150_766-143del
ENST00000476662.1:n.216-150_216-143del
NM_000526.4:c.766-150_766-143del	NP_000517.2:n.766-150_766-143del
NM_000526.5:c.766-150_766-143del MANE Select	NP_000517.3:n.766-150_766-143del