Canonical Allele Identifier: CA626215428

Gene: KRT14

Linked Data

• dbSNP Id: rs1442491225
• gnomAD v2: 17-39739932-C-CA
• gnomAD v4: 17-41583680-C-CA
• COSMIC: COSM5490702
• MyVariant Identifiers: chr17:g.39739932_39739933insA (hg19) ; chr17:g.41583680_41583681insA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583686dup , CM000679.2:g.41583686dup	GRCh38
NC_000017.10:g.39739938dup , CM000679.1:g.39739938dup	GRCh37
NC_000017.9:g.36993464dup	NCBI36
NG_008624.1:g.8215dup

Transcript Alleles

HGVS	Amino-acid change
ENST00000167586.7:c.928-5dup MANE Select	ENSP00000167586.6:n.928-5dup
ENST00000167586.6:c.928-5dup	ENSP00000167586.6:n.928-5dup
ENST00000476662.1:n.378-5dup
NM_000526.4:c.928-5dup	NP_000517.2:n.928-5dup
NM_000526.5:c.928-5dup MANE Select	NP_000517.3:n.928-5dup