Canonical Allele Identifier: CA2787135255
Gene: MTPAP HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313504T>C , CM000672.2:g.30313504T>C GRCh38
NC_000010.10:g.30602433T>C , CM000672.1:g.30602433T>C GRCh37
NC_000010.9:g.30642439T>C NCBI36
NG_028096.1:g.40835A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*105A>G MANE Select ENSP00000263063.3:n.*105A>G
ENST00000263063.8:c.*105A>G ENSP00000263063.3:n.*105A>G
ENST00000488290.5:n.3609A>G
NM_018109.3:c.*105A>G NP_060579.3:n.*105A>G
NM_018109.4:c.*105A>G MANE Select NP_060579.3:n.*105A>G