Canonical Allele Identifier: CA1899314216
Gene: MTPAP HGNC NCBI

Linked Data

dbSNP Id: rs1840635800
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30314306C>T , CM000672.2:g.30314306C>T GRCh38
NC_000010.10:g.30603235C>T , CM000672.1:g.30603235C>T GRCh37
NC_000010.9:g.30643241C>T NCBI36
NG_028096.1:g.40033G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1387-335G>A MANE Select ENSP00000263063.3:n.1387-335G>A
ENST00000263063.8:c.1387-335G>A ENSP00000263063.3:n.1387-335G>A
ENST00000488290.5:n.3142-335G>A
NM_018109.3:c.1387-335G>A NP_060579.3:n.1387-335G>A
NM_018109.4:c.1387-335G>A MANE Select NP_060579.3:n.1387-335G>A
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Search 100 bp 3'