Canonical Allele Identifier: CA2260085745

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584067_41584072delinsCTCTTT , CM000679.2:g.41584067_41584072delinsCTCTTT	GRCh38
NC_000017.10:g.39740319_39740324delinsCTCTTT , CM000679.1:g.39740319_39740324delinsCTCTTT	GRCh37
NC_000017.9:g.36993845_36993850delinsCTCTTT	NCBI36
NG_008624.1:g.7824_7829delinsAAAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-151_766-146delinsAAAGAG MANE Select	ENSP00000167586.6:n.766-151_766-146delinsAAAGAG
ENST00000167586.6:c.766-151_766-146delinsAAAGAG	ENSP00000167586.6:n.766-151_766-146delinsAAAGAG
ENST00000476662.1:n.216-151_216-146delinsAAAGAG
NM_000526.4:c.766-151_766-146delinsAAAGAG	NP_000517.2:n.766-151_766-146delinsAAAGAG
NM_000526.5:c.766-151_766-146delinsAAAGAG MANE Select	NP_000517.3:n.766-151_766-146delinsAAAGAG