Canonical Allele Identifier: CA2260085549

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583738T= , CM000679.2:g.41583738T=	GRCh38
NC_000017.10:g.39739990T= , CM000679.1:g.39739990T=	GRCh37
NC_000017.9:g.36993516T=	NCBI36
NG_008624.1:g.8158A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.927+22A= MANE Select	ENSP00000167586.6:n.927+22A=
ENST00000167586.6:c.927+22A=	ENSP00000167586.6:n.927+22A=
ENST00000476662.1:n.377+22A=
NM_000526.4:c.927+22A=	NP_000517.2:n.927+22A=
NM_000526.5:c.927+22A= MANE Select	NP_000517.3:n.927+22A=