Canonical Allele Identifier: CA8562505
Gene: KRT14 HGNC NCBI

Linked Data

dbSNP Id: rs768175939
ExAC: 17:39739726 G / GA
gnomAD v2: 17-39739726-G-GA
gnomAD v3: 17-41583474-G-GA
gnomAD v4: 17-41583474-G-GA
MyVariant Identifiers: chr17:g.39739726_39739727insA (hg19) chr17:g.41583474_41583475insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583476dup , CM000679.2:g.41583476dup GRCh38
NC_000017.10:g.39739728dup , CM000679.1:g.39739728dup GRCh37
NC_000017.9:g.36993254dup NCBI36
NG_008624.1:g.8421dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.1054-20dup MANE Select ENSP00000167586.6:n.1054-20dup
ENST00000167586.6:c.1054-20dup ENSP00000167586.6:n.1054-20dup
ENST00000476662.1:n.504-20dup
NM_000526.4:c.1054-20dup NP_000517.2:n.1054-20dup
NM_000526.5:c.1054-20dup MANE Select NP_000517.3:n.1054-20dup
Search 100 bp 5'
Search 100 bp 3'