Canonical Allele Identifier: CA8562753

Gene: KRT14

Linked Data

• dbSNP Id: rs779907477
• ExAC: 17:39742787 AAAGCCACCACCC / A
• gnomAD v4: 17-41586535-AAAGCCACCACCC-A
• MyVariant Identifiers: chr17:g.39742788_39742799del (hg19) ; chr17:g.41586536_41586547del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41586542_41586553del , CM000679.2:g.41586542_41586553del	GRCh38
NC_000017.10:g.39742794_39742805del , CM000679.1:g.39742794_39742805del	GRCh37
NC_000017.9:g.36996320_36996331del	NCBI36
NG_008624.1:g.5349_5360del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.288_299del MANE Select	ENSP00000167586.6:p.Leu96_Gly99del
ENST00000167586.6:c.288_299del	ENSP00000167586.6:p.Leu96_Gly99del
NM_000526.4:c.288_299del	NP_000517.2:p.Leu96_Gly99del
NM_000526.5:c.288_299del MANE Select	NP_000517.3:p.Leu96_Gly99del