Canonical Allele Identifier: CA480069611
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52910456G>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52516672G>C , CM000674.2:g.52516672G>C GRCh38
NC_000012.11:g.52910456G>C , CM000674.1:g.52910456G>C GRCh37
NC_000012.10:g.51196723G>C NCBI36
NG_008297.1:g.8788C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.1404C>G MANE Select ENSP00000252242.4:p.Ala468=
ENST00000252242.8:c.1404C>G ENSP00000252242.4:p.Ala468=
ENST00000548409.5:c.526C>G
ENST00000549511.5:n.611C>G
ENST00000552629.5:n.1502C>G
NM_000424.3:c.1404C>G NP_000415.2:p.Ala468=
NM_000424.4:c.1404C>G MANE Select NP_000415.2:p.Ala468=
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