Canonical Allele Identifier: CA626215537

Gene: KRT14

Linked Data

• dbSNP Id: rs200977988
• gnomAD v2: 17-39740303-ATCTC-A
• gnomAD v3: 17-41584051-ATCTC-A
• gnomAD v4: 17-41584051-ATCTC-A
• MyVariant Identifiers: chr17:g.39740304_39740307del (hg19) ; chr17:g.41584052_41584055del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584067_41584070del , CM000679.2:g.41584067_41584070del	GRCh38
NC_000017.10:g.39740319_39740322del , CM000679.1:g.39740319_39740322del	GRCh37
NC_000017.9:g.36993845_36993848del	NCBI36
NG_008624.1:g.7841_7844del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-134_766-131del MANE Select	ENSP00000167586.6:n.766-134_766-131del
ENST00000167586.6:c.766-134_766-131del	ENSP00000167586.6:n.766-134_766-131del
ENST00000476662.1:n.216-134_216-131del
NM_000526.4:c.766-134_766-131del	NP_000517.2:n.766-134_766-131del
NM_000526.5:c.766-134_766-131del MANE Select	NP_000517.3:n.766-134_766-131del