Canonical Allele Identifier: CA8562651
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs556488730
ExAC: 17:39740635 A / G
gnomAD v2: 17-39740635-A-G
gnomAD v3: 17-41584383-A-G
gnomAD v4: 17-41584383-A-G
MyVariant Identifiers: chr17:g.39740635A>G (hg19) chr17:g.41584383A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41584383A>G , CM000679.2:g.41584383A>G GRCh38
NC_000017.10:g.39740635A>G , CM000679.1:g.39740635A>G GRCh37
NC_000017.9:g.36994161A>G NCBI36
NG_008624.1:g.7513T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.639T>C MANE Select ENSP00000167586.6:p.Ser213=
ENST00000167586.6:c.639T>C ENSP00000167586.6:p.Ser213=
ENST00000476662.1:n.89T>C
NM_000526.4:c.639T>C NP_000517.2:p.Ser213=
NM_000526.5:c.639T>C MANE Select NP_000517.3:p.Ser213=
Search 100 bp 5'
Search 100 bp 3'