Canonical Allele Identifier: CA479848551
Gene: KRT5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52914018A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52520234A>C , CM000674.2:g.52520234A>C GRCh38
NC_000012.11:g.52914018A>C , CM000674.1:g.52914018A>C GRCh37
NC_000012.10:g.51200285A>C NCBI36
NG_008297.1:g.5226T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000252242.9:c.63T>G MANE Select ENSP00000252242.4:p.Ser21=
ENST00000252242.8:c.63T>G ENSP00000252242.4:p.Ser21=
ENST00000546577.1:c.63T>G ENSP00000449651.1:p.Ser21=
ENST00000549420.1:c.43+20T>G ENSP00000447209.1:n.43+20T>G
ENST00000551275.1:c.63T>G ENSP00000448041.1:p.Ser21=
ENST00000552629.5:n.161T>G
NM_000424.3:c.63T>G NP_000415.2:p.Ser21=
NM_000424.4:c.63T>G MANE Select NP_000415.2:p.Ser21=
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