Canonical Allele Identifier: CA376434650
Gene: MTPAP HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.30602795A>T (hg19) chr10:g.30313866A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313866A>T , CM000672.2:g.30313866A>T GRCh38
NC_000010.10:g.30602795A>T , CM000672.1:g.30602795A>T GRCh37
NC_000010.9:g.30642801A>T NCBI36
NG_028096.1:g.40473T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1492T>A MANE Select ENSP00000263063.3:p.Phe498Ile
ENST00000263063.8:c.1492T>A ENSP00000263063.3:p.Phe498Ile
ENST00000488290.5:n.3247T>A
NM_018109.3:c.1492T>A NP_060579.3:p.Phe498Ile
NM_018109.4:c.1492T>A MANE Select NP_060579.3:p.Phe498Ile
Search 100 bp 5'
Search 100 bp 3'