Canonical Allele Identifier: CA2036511448
Gene: KRT75 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433798C= , CM000674.2:g.52433798C= GRCh38
NC_000012.11:g.52827582C= , CM000674.1:g.52827582C= GRCh37
NC_000012.10:g.51113849C= NCBI36
NG_008403.1:g.5529G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.498+9G= MANE Select ENSP00000252245.5:n.498+9G=
ENST00000252245.5:c.498+9G= ENSP00000252245.5:n.498+9G=
NM_004693.2:c.498+9G= NP_004684.2:n.498+9G=
NM_004693.3:c.498+9G= MANE Select NP_004684.2:n.498+9G=
Search 100 bp 5'
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