Canonical Allele Identifier: CA2637835049

Gene: KRT14

Linked Data

• gnomAD v4: 17-41583680-CAA-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41583685_41583686del , CM000679.2:g.41583685_41583686del	GRCh38
NC_000017.10:g.39739937_39739938del , CM000679.1:g.39739937_39739938del	GRCh37
NC_000017.9:g.36993463_36993464del	NCBI36
NG_008624.1:g.8214_8215del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.928-6_928-5del MANE Select	ENSP00000167586.6:n.928-6_928-5del
ENST00000167586.6:c.928-6_928-5del	ENSP00000167586.6:n.928-6_928-5del
ENST00000476662.1:n.378-6_378-5del
NM_000526.4:c.928-6_928-5del	NP_000517.2:n.928-6_928-5del
NM_000526.5:c.928-6_928-5del MANE Select	NP_000517.3:n.928-6_928-5del