Canonical Allele Identifier: CA1899313819
Gene: MTPAP HGNC NCBI

Linked Data

dbSNP Id: rs898044538
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313397T>A , CM000672.2:g.30313397T>A GRCh38
NC_000010.10:g.30602326T>A , CM000672.1:g.30602326T>A GRCh37
NC_000010.9:g.30642332T>A NCBI36
NG_028096.1:g.40942A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*212A>T MANE Select ENSP00000263063.3:n.*212A>T
ENST00000263063.8:c.*212A>T ENSP00000263063.3:n.*212A>T
ENST00000488290.5:n.3716A>T
NM_018109.3:c.*212A>T NP_060579.3:n.*212A>T
NM_018109.4:c.*212A>T MANE Select NP_060579.3:n.*212A>T
Search 100 bp 5'
Search 100 bp 3'