Canonical Allele Identifier: CA384988616
Gene: KRT4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.53203212G>C (hg19) chr12:g.52809428G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52809428G>C , CM000674.2:g.52809428G>C GRCh38
NC_000012.11:g.53203212G>C , CM000674.1:g.53203212G>C GRCh37
NC_000012.10:g.51489479G>C NCBI36
NG_007380.1:g.10124C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.789C>G MANE Select ENSP00000448220.1:p.Asp263Glu
ENST00000548097.5:c.*301C>G ENSP00000449755.1:n.*301C>G
ENST00000549295.1:n.223C>G
ENST00000551956.1:c.789C>G ENSP00000448220.1:p.Asp263Glu
ENST00000552668.1:c.*194C>G ENSP00000447320.1:n.*194C>G
NM_002272.3:c.789C>G NP_002263.3:p.Asp263Glu
NM_002272.4:c.789C>G MANE Select NP_002263.3:p.Asp263Glu
Search 100 bp 5'
Search 100 bp 3'