Canonical Allele Identifier: CA2809495844
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583744C>G , CM000679.2:g.41583744C>G GRCh38
NC_000017.10:g.39739996C>G , CM000679.1:g.39739996C>G GRCh37
NC_000017.9:g.36993522C>G NCBI36
NG_008624.1:g.8152G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000167586.7:c.927+16G>C MANE Select ENSP00000167586.6:n.927+16G>C
ENST00000167586.6:c.927+16G>C ENSP00000167586.6:n.927+16G>C
ENST00000476662.1:n.377+16G>C
NM_000526.4:c.927+16G>C NP_000517.2:n.927+16G>C
NM_000526.5:c.927+16G>C MANE Select NP_000517.3:n.927+16G>C
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