Canonical Allele Identifier: CA8562563

Gene: KRT14

Linked Data

• dbSNP Id: rs776040325
• ExAC: 17:39739937 AAG / A
• gnomAD v2: 17-39739937-AAG-A
• gnomAD v3: 17-41583685-AAG-A
• gnomAD v4: 17-41583685-AAG-A
• MyVariant Identifiers: chr17:g.39739938_39739939del (hg19) ; chr17:g.41583687_41583688del (hg38) ; chr17:g.41583686_41583687del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583689_41583690del , CM000679.2:g.41583689_41583690del	GRCh38
NC_000017.10:g.39739941_39739942del , CM000679.1:g.39739941_39739942del	GRCh37
NC_000017.9:g.36993467_36993468del	NCBI36
NG_008624.1:g.8209_8210del

Transcript Alleles

HGVS	Amino-acid change
ENST00000167586.7:c.928-11_928-10del MANE Select	ENSP00000167586.6:n.928-11_928-10del
ENST00000167586.6:c.928-11_928-10del	ENSP00000167586.6:n.928-11_928-10del
ENST00000476662.1:n.378-11_378-10del
NM_000526.4:c.928-11_928-10del	NP_000517.2:n.928-11_928-10del
NM_000526.5:c.928-11_928-10del MANE Select	NP_000517.3:n.928-11_928-10del