Canonical Allele Identifier: CA772038475
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1396940091
MyVariant Identifiers: chr17:g.39739721A>G (hg19) chr17:g.41583469A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583469A>G , CM000679.2:g.41583469A>G GRCh38
NC_000017.10:g.39739721A>G , CM000679.1:g.39739721A>G GRCh37
NC_000017.9:g.36993247A>G NCBI36
NG_008624.1:g.8427T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1054-14T>C MANE Select ENSP00000167586.6:n.1054-14T>C
ENST00000167586.6:c.1054-14T>C ENSP00000167586.6:n.1054-14T>C
ENST00000476662.1:n.504-14T>C
NM_000526.4:c.1054-14T>C NP_000517.2:n.1054-14T>C
NM_000526.5:c.1054-14T>C MANE Select NP_000517.3:n.1054-14T>C
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