Canonical Allele Identifier: CA480076166
Gene: KRT4 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.53207729A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52813945A>C , CM000674.2:g.52813945A>C GRCh38
NC_000012.11:g.53207729A>C , CM000674.1:g.53207729A>C GRCh37
NC_000012.10:g.51493996A>C NCBI36
NG_007380.1:g.5607T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000551956.2:c.114T>G MANE Select ENSP00000448220.1:p.Gly38=
ENST00000548097.5:c.114T>G ENSP00000449755.1:p.Gly38=
ENST00000551956.1:c.114T>G ENSP00000448220.1:p.Gly38=
ENST00000552668.1:c.114T>G ENSP00000447320.1:p.Gly38=
NM_002272.3:c.114T>G NP_002263.3:p.Gly38=
NM_002272.4:c.114T>G MANE Select NP_002263.3:p.Gly38=
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