Canonical Allele Identifier: CA2036511434
Gene: KRT75 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433784G= , CM000674.2:g.52433784G= GRCh38
NC_000012.11:g.52827568G= , CM000674.1:g.52827568G= GRCh37
NC_000012.10:g.51113835G= NCBI36
NG_008403.1:g.5543C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.498+23C= MANE Select ENSP00000252245.5:n.498+23C=
ENST00000252245.5:c.498+23C= ENSP00000252245.5:n.498+23C=
NM_004693.2:c.498+23C= NP_004684.2:n.498+23C=
NM_004693.3:c.498+23C= MANE Select NP_004684.2:n.498+23C=
Search 100 bp 5'
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