Canonical Allele Identifier: CA384973722
Gene: KRT75 HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.52827661T>A (hg19) chr12:g.52433877T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.52433877T>A , CM000674.2:g.52433877T>A GRCh38
NC_000012.11:g.52827661T>A , CM000674.1:g.52827661T>A GRCh37
NC_000012.10:g.51113928T>A NCBI36
NG_008403.1:g.5450A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000252245.6:c.428A>T MANE Select ENSP00000252245.5:p.Gln143Leu
ENST00000252245.5:c.428A>T ENSP00000252245.5:p.Gln143Leu
NM_004693.2:c.428A>T NP_004684.2:p.Gln143Leu
NM_004693.3:c.428A>T MANE Select NP_004684.2:p.Gln143Leu
Search 100 bp 5'
Search 100 bp 3'