Canonical Allele Identifier: CA626215561

Gene: KRT14

Linked Data

• dbSNP Id: rs1158275682
• gnomAD v2: 17-39740338-T-TC
• gnomAD v3: 17-41584086-T-TC
• gnomAD v4: 17-41584086-T-TC
• MyVariant Identifiers: chr17:g.39740338_39740339insC (hg19) ; chr17:g.41584086_41584087insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584086_41584087insC , CM000679.2:g.41584086_41584087insC	GRCh38
NC_000017.10:g.39740338_39740339insC , CM000679.1:g.39740338_39740339insC	GRCh37
NC_000017.9:g.36993864_36993865insC	NCBI36
NG_008624.1:g.7809_7810insG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-166_766-165insG MANE Select	ENSP00000167586.6:n.766-166_766-165insG
ENST00000167586.6:c.766-166_766-165insG	ENSP00000167586.6:n.766-166_766-165insG
ENST00000476662.1:n.216-166_216-165insG
NM_000526.4:c.766-166_766-165insG	NP_000517.2:n.766-166_766-165insG
NM_000526.5:c.766-166_766-165insG MANE Select	NP_000517.3:n.766-166_766-165insG