Canonical Allele Identifier: CA2036511432
Gene: KRT75 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433783G= , CM000674.2:g.52433783G= GRCh38
NC_000012.11:g.52827567G= , CM000674.1:g.52827567G= GRCh37
NC_000012.10:g.51113834G= NCBI36
NG_008403.1:g.5544C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.498+24C= MANE Select ENSP00000252245.5:n.498+24C=
ENST00000252245.5:c.498+24C= ENSP00000252245.5:n.498+24C=
NM_004693.2:c.498+24C= NP_004684.2:n.498+24C=
NM_004693.3:c.498+24C= MANE Select NP_004684.2:n.498+24C=
Search 100 bp 5'
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