Canonical Allele Identifier: CA468799008
Gene: MTPAP HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.30602871A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313942A>G , CM000672.2:g.30313942A>G GRCh38
NC_000010.10:g.30602871A>G , CM000672.1:g.30602871A>G GRCh37
NC_000010.9:g.30642877A>G NCBI36
NG_028096.1:g.40397T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1416T>C MANE Select ENSP00000263063.3:p.Ser472=
ENST00000263063.8:c.1416T>C ENSP00000263063.3:p.Ser472=
ENST00000488290.5:n.3171T>C
NM_018109.3:c.1416T>C NP_060579.3:p.Ser472=
NM_018109.4:c.1416T>C MANE Select NP_060579.3:p.Ser472=
Search 100 bp 5'
Search 100 bp 3'