Canonical Allele Identifier: CA290665094

Gene: KRT14

Linked Data

• dbSNP Id: rs1033811298
• gnomAD v2: 17-39740331-T-C
• gnomAD v3: 17-41584079-T-C
• gnomAD v4: 17-41584079-T-C
• MyVariant Identifiers: chr17:g.39740331T>C (hg19) ; chr17:g.41584079T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.41584079T>C , CM000679.2:g.41584079T>C	GRCh38
NC_000017.10:g.39740331T>C , CM000679.1:g.39740331T>C	GRCh37
NC_000017.9:g.36993857T>C	NCBI36
NG_008624.1:g.7817A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000167586.7:c.766-158A>G MANE Select	ENSP00000167586.6:n.766-158A>G
ENST00000167586.6:c.766-158A>G	ENSP00000167586.6:n.766-158A>G
ENST00000476662.1:n.216-158A>G
NM_000526.4:c.766-158A>G	NP_000517.2:n.766-158A>G
NM_000526.5:c.766-158A>G MANE Select	NP_000517.3:n.766-158A>G