Canonical Allele Identifier: CA8562488
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs768112503
ExAC: 17:39739621 C / G
gnomAD v2: 17-39739621-C-G
gnomAD v3: 17-41583369-C-G
gnomAD v4: 17-41583369-C-G
MyVariant Identifiers: chr17:g.39739621C>G (hg19) chr17:g.41583369C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583369C>G , CM000679.2:g.41583369C>G GRCh38
NC_000017.10:g.39739621C>G , CM000679.1:g.39739621C>G GRCh37
NC_000017.9:g.36993147C>G NCBI36
NG_008624.1:g.8527G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1140G>C MANE Select ENSP00000167586.6:p.Val380=
ENST00000167586.6:c.1140G>C ENSP00000167586.6:p.Val380=
ENST00000441550.2:n.87G>C
ENST00000476662.1:n.590G>C
NM_000526.4:c.1140G>C NP_000517.2:p.Val380=
NM_000526.5:c.1140G>C MANE Select NP_000517.3:p.Val380=
Search 100 bp 5'
Search 100 bp 3'