Canonical Allele Identifier: CA2260085483

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583609G= , CM000679.2:g.41583609G=	GRCh38
NC_000017.10:g.39739861G= , CM000679.1:g.39739861G=	GRCh37
NC_000017.9:g.36993387G=	NCBI36
NG_008624.1:g.8287C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000167586.7:c.995C= MANE Select	ENSP00000167586.6:p.Ser332=
ENST00000167586.6:c.995C=	ENSP00000167586.6:p.Ser332=
ENST00000476662.1:n.445C=
NM_000526.4:c.995C=	NP_000517.2:p.Ser332=
NM_000526.5:c.995C= MANE Select	NP_000517.3:p.Ser332=