Canonical Allele Identifier: CA290664696
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs936100
gnomAD v2: 17-39739272-T-A
gnomAD v3: 17-41583020-T-A
gnomAD v4: 17-41583020-T-A
MyVariant Identifiers: chr17:g.39739272T>A (hg19) chr17:g.41583020T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583020T>A , CM000679.2:g.41583020T>A GRCh38
NC_000017.10:g.39739272T>A , CM000679.1:g.39739272T>A GRCh37
NC_000017.9:g.36992798T>A NCBI36
NG_008624.1:g.8876A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000167586.7:c.1321+74A>T MANE Select ENSP00000167586.6:n.1321+74A>T
ENST00000167586.6:c.1321+74A>T ENSP00000167586.6:n.1321+74A>T
ENST00000441550.2:n.342A>T
NM_000526.4:c.1321+74A>T NP_000517.2:n.1321+74A>T
NM_000526.5:c.1321+74A>T MANE Select NP_000517.3:n.1321+74A>T
Search 100 bp 5'
Search 100 bp 3'