Canonical Allele Identifier: CA2809495712

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41582981_41582982del , CM000679.2:g.41582981_41582982del	GRCh38
NC_000017.10:g.39739233_39739234del , CM000679.1:g.39739233_39739234del	GRCh37
NC_000017.9:g.36992759_36992760del	NCBI36
NG_008624.1:g.8914_8915del

Transcript Alleles

HGVS	Amino-acid change
ENST00000167586.7:c.1321+112_1321+113del MANE Select	ENSP00000167586.6:n.1321+112_1321+113del
ENST00000167586.6:c.1321+112_1321+113del	ENSP00000167586.6:n.1321+112_1321+113del
ENST00000441550.2:n.380_381del
NM_000526.4:c.1321+112_1321+113del	NP_000517.2:n.1321+112_1321+113del
NM_000526.5:c.1321+112_1321+113del MANE Select	NP_000517.3:n.1321+112_1321+113del