Canonical Allele Identifier: CA205301304
Gene: MTPAP HGNC NCBI

Linked Data

dbSNP Id: rs867422231
MyVariant Identifiers: chr10:g.30603180G>C (hg19) chr10:g.30314251G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30314251G>C , CM000672.2:g.30314251G>C GRCh38
NC_000010.10:g.30603180G>C , CM000672.1:g.30603180G>C GRCh37
NC_000010.9:g.30643186G>C NCBI36
NG_028096.1:g.40088C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1387-280C>G MANE Select ENSP00000263063.3:n.1387-280C>G
ENST00000263063.8:c.1387-280C>G ENSP00000263063.3:n.1387-280C>G
ENST00000488290.5:n.3142-280C>G
NM_018109.3:c.1387-280C>G NP_060579.3:n.1387-280C>G
NM_018109.4:c.1387-280C>G MANE Select NP_060579.3:n.1387-280C>G
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