Canonical Allele Identifier: CA626215536

Gene: KRT14

Linked Data

• dbSNP Id: rs1358769106
• gnomAD v2: 17-39740302-AATCTCTCTCTCTCT-A
• gnomAD v4: 17-41584050-AATCTCTCTCTCTCT-A
• MyVariant Identifiers: chr17:g.39740303_39740316del (hg19) ; chr17:g.41584051_41584064del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584051_41584064del , CM000679.2:g.41584051_41584064del	GRCh38
NC_000017.10:g.39740303_39740316del , CM000679.1:g.39740303_39740316del	GRCh37
NC_000017.9:g.36993829_36993842del	NCBI36
NG_008624.1:g.7832_7845del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-143_766-130del MANE Select	ENSP00000167586.6:n.766-143_766-130del
ENST00000167586.6:c.766-143_766-130del	ENSP00000167586.6:n.766-143_766-130del
ENST00000476662.1:n.216-143_216-130del
NM_000526.4:c.766-143_766-130del	NP_000517.2:n.766-143_766-130del
NM_000526.5:c.766-143_766-130del MANE Select	NP_000517.3:n.766-143_766-130del