Canonical Allele Identifier: CA2260085722

Gene: KRT14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584051_41584057delinsATCTCTC , CM000679.2:g.41584051_41584057delinsATCTCTC	GRCh38
NC_000017.10:g.39740303_39740309delinsATCTCTC , CM000679.1:g.39740303_39740309delinsATCTCTC	GRCh37
NC_000017.9:g.36993829_36993835delinsATCTCTC	NCBI36
NG_008624.1:g.7839_7845delinsGAGAGAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-136_766-130delinsGAGAGAT MANE Select	ENSP00000167586.6:n.766-136_766-130delinsGAGAGAT
ENST00000167586.6:c.766-136_766-130delinsGAGAGAT	ENSP00000167586.6:n.766-136_766-130delinsGAGAGAT
ENST00000476662.1:n.216-136_216-130delinsGAGAGAT
NM_000526.4:c.766-136_766-130delinsGAGAGAT	NP_000517.2:n.766-136_766-130delinsGAGAGAT
NM_000526.5:c.766-136_766-130delinsGAGAGAT MANE Select	NP_000517.3:n.766-136_766-130delinsGAGAGAT