Canonical Allele Identifier: CA2260085265

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583194T= , CM000679.2:g.41583194T=	GRCh38
NC_000017.10:g.39739446T= , CM000679.1:g.39739446T=	GRCh37
NC_000017.9:g.36992972T=	NCBI36
NG_008624.1:g.8702A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.1274+41A= MANE Select	ENSP00000167586.6:n.1274+41A=
ENST00000167586.6:c.1274+41A=	ENSP00000167586.6:n.1274+41A=
ENST00000441550.2:n.221+41A=
NM_000526.4:c.1274+41A=	NP_000517.2:n.1274+41A=
NM_000526.5:c.1274+41A= MANE Select	NP_000517.3:n.1274+41A=