Canonical Allele Identifier: CA480067606
Gene: KRT75 HGNC NCBI

Linked Data

COSMIC: COSM3462254
MyVariant Identifiers: chr12:g.52827645C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433861C>T , CM000674.2:g.52433861C>T GRCh38
NC_000012.11:g.52827645C>T , CM000674.1:g.52827645C>T GRCh37
NC_000012.10:g.51113912C>T NCBI36
NG_008403.1:g.5466G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.444G>A MANE Select ENSP00000252245.5:p.Glu148=
ENST00000252245.5:c.444G>A ENSP00000252245.5:p.Glu148=
NM_004693.2:c.444G>A NP_004684.2:p.Glu148=
NM_004693.3:c.444G>A MANE Select NP_004684.2:p.Glu148=
Search 100 bp 5'
Search 100 bp 3'