Canonical Allele Identifier: CA384991271
Gene: KRT4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.53207748G>T (hg19) chr12:g.52813964G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52813964G>T , CM000674.2:g.52813964G>T GRCh38
NC_000012.11:g.53207748G>T , CM000674.1:g.53207748G>T GRCh37
NC_000012.10:g.51494015G>T NCBI36
NG_007380.1:g.5588C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000551956.2:c.95C>A MANE Select ENSP00000448220.1:p.Ser32Ter
ENST00000548097.5:c.95C>A ENSP00000449755.1:p.Ser32Ter
ENST00000551956.1:c.95C>A ENSP00000448220.1:p.Ser32Ter
ENST00000552668.1:c.95C>A ENSP00000447320.1:p.Ser32Ter
NM_002272.3:c.95C>A NP_002263.3:p.Ser32Ter
NM_002272.4:c.95C>A MANE Select NP_002263.3:p.Ser32Ter
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