Canonical Allele Identifier: CA384929716
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52913736A>C (hg19) chr12:g.52519952A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52519952A>C , CM000674.2:g.52519952A>C GRCh38
NC_000012.11:g.52913736A>C , CM000674.1:g.52913736A>C GRCh37
NC_000012.10:g.51200003A>C NCBI36
NG_008297.1:g.5508T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.345T>G MANE Select ENSP00000252242.4:p.Phe115Leu
ENST00000252242.8:c.345T>G ENSP00000252242.4:p.Phe115Leu
ENST00000546577.1:c.345T>G ENSP00000449651.1:p.Phe115Leu
ENST00000549420.1:c.44-29T>G ENSP00000447209.1:n.44-29T>G
ENST00000551275.1:c.240T>G ENSP00000448041.1:p.Phe80Leu
ENST00000552629.5:n.443T>G
NM_000424.3:c.345T>G NP_000415.2:p.Phe115Leu
NM_000424.4:c.345T>G MANE Select NP_000415.2:p.Phe115Leu
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