Canonical Allele Identifier: CA2571857346

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583520_41583521insCGCG , CM000679.2:g.41583520_41583521insCGCG	GRCh38
NC_000017.10:g.39739772_39739773insCGCG , CM000679.1:g.39739772_39739773insCGCG	GRCh37
NC_000017.9:g.36993298_36993299insCGCG	NCBI36
NG_008624.1:g.8376_8377insGCGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.1053+31_1053+32insGCGC MANE Select	ENSP00000167586.6:n.1053+31_1053+32insGCGC
ENST00000167586.6:c.1053+31_1053+32insGCGC	ENSP00000167586.6:n.1053+31_1053+32insGCGC
ENST00000476662.1:n.503+31_503+32insGCGC
NM_000526.4:c.1053+31_1053+32insGCGC	NP_000517.2:n.1053+31_1053+32insGCGC
NM_000526.5:c.1053+31_1053+32insGCGC MANE Select	NP_000517.3:n.1053+31_1053+32insGCGC