Canonical Allele Identifier: CA8562650
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs75795684
ExAC: 17:39740629 T / G
gnomAD v2: 17-39740629-T-G
gnomAD v4: 17-41584377-T-G
MyVariant Identifiers: chr17:g.39740629T>G (hg19) chr17:g.41584377T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584377T>G , CM000679.2:g.41584377T>G GRCh38
NC_000017.10:g.39740629T>G , CM000679.1:g.39740629T>G GRCh37
NC_000017.9:g.36994155T>G NCBI36
NG_008624.1:g.7519A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.645A>C MANE Select ENSP00000167586.6:p.Glu215Asp
ENST00000167586.6:c.645A>C ENSP00000167586.6:p.Glu215Asp
ENST00000476662.1:n.95A>C
NM_000526.4:c.645A>C NP_000517.2:p.Glu215Asp
NM_000526.5:c.645A>C MANE Select NP_000517.3:p.Glu215Asp
Search 100 bp 5'
Search 100 bp 3'