Canonical Allele Identifier: CA919841691

Gene: KRT14

Linked Data

• dbSNP Id: rs1567737207

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584424_41584426del , CM000679.2:g.41584424_41584426del	GRCh38
NC_000017.10:g.39740676_39740678del , CM000679.1:g.39740676_39740678del	GRCh37
NC_000017.9:g.36994202_36994204del	NCBI36
NG_008624.1:g.7471_7473del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.609-12_609-10del MANE Select	ENSP00000167586.6:n.609-12_609-10del
ENST00000167586.6:c.609-12_609-10del	ENSP00000167586.6:n.609-12_609-10del
ENST00000476662.1:n.47_49del
NM_000526.4:c.609-12_609-10del	NP_000517.2:n.609-12_609-10del
NM_000526.5:c.609-12_609-10del MANE Select	NP_000517.3:n.609-12_609-10del