Canonical Allele Identifier: CA626215527

Gene: KRT14

Linked Data

• dbSNP Id: rs1567736979
• gnomAD v2: 17-39740285-TTCTCTCTCTCTCTCTCAATCTCTC-T
• gnomAD v3: 17-41584033-TTCTCTCTCTCTCTCTCAATCTCTC-T
• gnomAD v4: 17-41584033-TTCTCTCTCTCTCTCTCAATCTCTC-T
• MyVariant Identifiers: chr17:g.39740286_39740309del (hg19) ; chr17:g.41584034_41584057del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584047_41584070del , CM000679.2:g.41584047_41584070del	GRCh38
NC_000017.10:g.39740299_39740322del , CM000679.1:g.39740299_39740322del	GRCh37
NC_000017.9:g.36993825_36993848del	NCBI36
NG_008624.1:g.7839_7862del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-136_766-113del MANE Select	ENSP00000167586.6:n.766-136_766-113del
ENST00000167586.6:c.766-136_766-113del	ENSP00000167586.6:n.766-136_766-113del
ENST00000476662.1:n.216-136_216-113del
NM_000526.4:c.766-136_766-113del	NP_000517.2:n.766-136_766-113del
NM_000526.5:c.766-136_766-113del MANE Select	NP_000517.3:n.766-136_766-113del