Canonical Allele Identifier: CA626215544

Gene: KRT14

Linked Data

• dbSNP Id: rs1907438530
• gnomAD v2: 17-39740304-TCTCTCTCTCTCTCTCTC-T
• gnomAD v3: 17-41584052-TCTCTCTCTCTCTCTCTC-T
• gnomAD v4: 17-41584052-TCTCTCTCTCTCTCTCTC-T
• MyVariant Identifiers: chr17:g.39740305_39740321del (hg19) ; chr17:g.41584053_41584069del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584053_41584069del , CM000679.2:g.41584053_41584069del	GRCh38
NC_000017.10:g.39740305_39740321del , CM000679.1:g.39740305_39740321del	GRCh37
NC_000017.9:g.36993831_36993847del	NCBI36
NG_008624.1:g.7827_7843del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-148_766-132del MANE Select	ENSP00000167586.6:n.766-148_766-132del
ENST00000167586.6:c.766-148_766-132del	ENSP00000167586.6:n.766-148_766-132del
ENST00000476662.1:n.216-148_216-132del
NM_000526.4:c.766-148_766-132del	NP_000517.2:n.766-148_766-132del
NM_000526.5:c.766-148_766-132del MANE Select	NP_000517.3:n.766-148_766-132del