Canonical Allele Identifier: CA480076301
Gene: KRT4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.53207818G>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52814034G>T , CM000674.2:g.52814034G>T GRCh38
NC_000012.11:g.53207818G>T , CM000674.1:g.53207818G>T GRCh37
NC_000012.10:g.51494085G>T NCBI36
NG_007380.1:g.5518C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.25C>A MANE Select ENSP00000448220.1:p.Arg9=
ENST00000548097.5:c.25C>A ENSP00000449755.1:p.Arg9=
ENST00000551956.1:c.25C>A ENSP00000448220.1:p.Arg9=
ENST00000552668.1:c.25C>A ENSP00000447320.1:p.Arg9=
NM_002272.3:c.25C>A NP_002263.3:p.Arg9=
NM_002272.4:c.25C>A MANE Select NP_002263.3:p.Arg9=
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