Canonical Allele Identifier: CA8562743
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs773422606
ExAC: 17:39742763 A / G
gnomAD v2: 17-39742763-A-G
gnomAD v3: 17-41586511-A-G
gnomAD v4: 17-41586511-A-G
MyVariant Identifiers: chr17:g.39742763A>G (hg19) chr17:g.41586511A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41586511A>G , CM000679.2:g.41586511A>G GRCh38
NC_000017.10:g.39742763A>G , CM000679.1:g.39742763A>G GRCh37
NC_000017.9:g.36996289A>G NCBI36
NG_008624.1:g.5385T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.324T>C MANE Select ENSP00000167586.6:p.Asp108=
ENST00000167586.6:c.324T>C ENSP00000167586.6:p.Asp108=
NM_000526.4:c.324T>C NP_000517.2:p.Asp108=
NM_000526.5:c.324T>C MANE Select NP_000517.3:p.Asp108=
Search 100 bp 5'
Search 100 bp 3'