Canonical Allele Identifier: CA216982
Community Standard Title: NM_000526.5(KRT14):c.815T>G (p.Met272Arg)
Gene: KRT14 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.41583872A>C , CM000679.2:g.41583872A>C GRCh38
NC_000017.10:g.39740124A>C , CM000679.1:g.39740124A>C GRCh37
NC_000017.9:g.36993650A>C NCBI36
NG_008624.1:g.8024T>G

Transcript Alleles

HGVS Amino-acid Change
NM_000526.5:c.815T>G MANE Select NP_000517.3:p.Met272Arg
ENST00000167586.7:c.815T>G MANE Select ENSP00000167586.6:p.Met272Arg
NM_000526.4:c.815T>G NP_000517.2:p.Met272Arg
ENST00000167586.6:c.815T>G ENSP00000167586.6:p.Met272Arg
ENST00000476662.1:n.265T>G
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