Canonical Allele Identifier: CA384985807
Gene: KRT4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.53201479A>C (hg19) chr12:g.52807695A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52807695A>C , CM000674.2:g.52807695A>C GRCh38
NC_000012.11:g.53201479A>C , CM000674.1:g.53201479A>C GRCh37
NC_000012.10:g.51487746A>C NCBI36
NG_007380.1:g.11857T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.1295T>G MANE Select ENSP00000448220.1:p.Leu432Trp
ENST00000548097.5:c.*807T>G ENSP00000449755.1:n.*807T>G
ENST00000551956.1:c.1295T>G ENSP00000448220.1:p.Leu432Trp
NM_002272.3:c.1295T>G NP_002263.3:p.Leu432Trp
NM_002272.4:c.1295T>G MANE Select NP_002263.3:p.Leu432Trp
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