Canonical Allele Identifier: CA2637835838

Gene: KRT14

Linked Data

• gnomAD v4: 17-41584061-C-CTG

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584062_41584063insGT , CM000679.2:g.41584062_41584063insGT	GRCh38
NC_000017.10:g.39740314_39740315insGT , CM000679.1:g.39740314_39740315insGT	GRCh37
NC_000017.9:g.36993840_36993841insGT	NCBI36
NG_008624.1:g.7834_7835insCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-141_766-140insCA MANE Select	ENSP00000167586.6:n.766-141_766-140insCA
ENST00000167586.6:c.766-141_766-140insCA	ENSP00000167586.6:n.766-141_766-140insCA
ENST00000476662.1:n.216-141_216-140insCA
NM_000526.4:c.766-141_766-140insCA	NP_000517.2:n.766-141_766-140insCA
NM_000526.5:c.766-141_766-140insCA MANE Select	NP_000517.3:n.766-141_766-140insCA