Canonical Allele Identifier: CA2809495333

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584609dup , CM000679.2:g.41584609dup	GRCh38
NC_000017.10:g.39740861dup , CM000679.1:g.39740861dup	GRCh37
NC_000017.9:g.36994387dup	NCBI36
NG_008624.1:g.7287dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.609-196dup MANE Select	ENSP00000167586.6:n.609-196dup
ENST00000167586.6:c.609-196dup	ENSP00000167586.6:n.609-196dup
NM_000526.4:c.609-196dup	NP_000517.2:n.609-196dup
NM_000526.5:c.609-196dup MANE Select	NP_000517.3:n.609-196dup