Canonical Allele Identifier: CA2576267714

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583055_41583057dup , CM000679.2:g.41583055_41583057dup	GRCh38
NC_000017.10:g.39739307_39739309dup , CM000679.1:g.39739307_39739309dup	GRCh37
NC_000017.9:g.36992833_36992835dup	NCBI36
NG_008624.1:g.8841_8843dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.1321+39_1321+41dup MANE Select	ENSP00000167586.6:n.1321+39_1321+41dup
ENST00000167586.6:c.1321+39_1321+41dup	ENSP00000167586.6:n.1321+39_1321+41dup
ENST00000441550.2:n.307_309dup
NM_000526.4:c.1321+39_1321+41dup	NP_000517.2:n.1321+39_1321+41dup
NM_000526.5:c.1321+39_1321+41dup MANE Select	NP_000517.3:n.1321+39_1321+41dup