Canonical Allele Identifier: CA376434219
Gene: MTPAP HGNC NCBI

Linked Data

COSMIC: COSM465596 COSM465597
MyVariant Identifiers: chr10:g.30602666A>G (hg19) chr10:g.30313737A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313737A>G , CM000672.2:g.30313737A>G GRCh38
NC_000010.10:g.30602666A>G , CM000672.1:g.30602666A>G GRCh37
NC_000010.9:g.30642672A>G NCBI36
NG_028096.1:g.40602T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263063.9:c.1621T>C MANE Select ENSP00000263063.3:p.Phe541Leu
ENST00000263063.8:c.1621T>C ENSP00000263063.3:p.Phe541Leu
ENST00000488290.5:n.3376T>C
NM_018109.3:c.1621T>C NP_060579.3:p.Phe541Leu
NM_018109.4:c.1621T>C MANE Select NP_060579.3:p.Phe541Leu
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Search 100 bp 3'