Canonical Allele Identifier: CA626215379

Gene: KRT14

Linked Data

• dbSNP Id: rs1402339191
• gnomAD v2: 17-39739314-G-GAGCCCAGGCCTGC
• gnomAD v4: 17-41583062-G-GAGCCCAGGCCTGC
• MyVariant Identifiers: chr17:g.39739314_39739315insAGCCCAGGCCTGC (hg19) ; chr17:g.41583062_41583063insAGCCCAGGCCTGC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583065_41583077dup , CM000679.2:g.41583065_41583077dup	GRCh38
NC_000017.10:g.39739317_39739329dup , CM000679.1:g.39739317_39739329dup	GRCh37
NC_000017.9:g.36992843_36992855dup	NCBI36
NG_008624.1:g.8821_8833dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.1321+19_1321+31dup MANE Select	ENSP00000167586.6:n.1321+19_1321+31dup
ENST00000167586.6:c.1321+19_1321+31dup	ENSP00000167586.6:n.1321+19_1321+31dup
ENST00000441550.2:n.287_299dup
NM_000526.4:c.1321+19_1321+31dup	NP_000517.2:n.1321+19_1321+31dup
NM_000526.5:c.1321+19_1321+31dup MANE Select	NP_000517.3:n.1321+19_1321+31dup