Canonical Allele Identifier: CA772037665
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1436658859
gnomAD v3: 17-41582989-A-C
gnomAD v4: 17-41582989-A-C
MyVariant Identifiers: chr17:g.39739241A>C (hg19) chr17:g.41582989A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41582989A>C , CM000679.2:g.41582989A>C GRCh38
NC_000017.10:g.39739241A>C , CM000679.1:g.39739241A>C GRCh37
NC_000017.9:g.36992767A>C NCBI36
NG_008624.1:g.8907T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1321+105T>G MANE Select ENSP00000167586.6:n.1321+105T>G
ENST00000167586.6:c.1321+105T>G ENSP00000167586.6:n.1321+105T>G
ENST00000441550.2:n.373T>G
NM_000526.4:c.1321+105T>G NP_000517.2:n.1321+105T>G
NM_000526.5:c.1321+105T>G MANE Select NP_000517.3:n.1321+105T>G
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