Canonical Allele Identifier: CA1899313905
Gene: MTPAP HGNC NCBI

Linked Data

dbSNP Id: rs1588710291
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313576C>A , CM000672.2:g.30313576C>A GRCh38
NC_000010.10:g.30602505C>A , CM000672.1:g.30602505C>A GRCh37
NC_000010.9:g.30642511C>A NCBI36
NG_028096.1:g.40763G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*33G>T MANE Select ENSP00000263063.3:n.*33G>T
ENST00000263063.8:c.*33G>T ENSP00000263063.3:n.*33G>T
ENST00000488290.5:n.3537G>T
NM_018109.3:c.*33G>T NP_060579.3:n.*33G>T
NM_018109.4:c.*33G>T MANE Select NP_060579.3:n.*33G>T
Search 100 bp 5'
Search 100 bp 3'