Canonical Allele Identifier: CA399483954
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs1166730746
gnomAD v2: 17-39743046-A-C
MyVariant Identifiers: chr17:g.39743046A>C (hg19) chr17:g.41586794A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586794A>C , CM000679.2:g.41586794A>C GRCh38
NC_000017.10:g.39743046A>C , CM000679.1:g.39743046A>C GRCh37
NC_000017.9:g.36996572A>C NCBI36
NG_008624.1:g.5102T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.41T>G MANE Select ENSP00000167586.6:p.Met14Arg
ENST00000167586.6:c.41T>G ENSP00000167586.6:p.Met14Arg
NM_000526.4:c.41T>G NP_000517.2:p.Met14Arg
NM_000526.5:c.41T>G MANE Select NP_000517.3:p.Met14Arg
Search 100 bp 5'
Search 100 bp 3'