Canonical Allele Identifier: CA663650027
Gene: MTPAP HGNC NCBI

Linked Data

dbSNP Id: rs1334534116
gnomAD v3: 10-30313551-G-A
gnomAD v4: 10-30313551-G-A
MyVariant Identifiers: chr10:g.30602480G>A (hg19) chr10:g.30313551G>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313551G>A , CM000672.2:g.30313551G>A GRCh38
NC_000010.10:g.30602480G>A , CM000672.1:g.30602480G>A GRCh37
NC_000010.9:g.30642486G>A NCBI36
NG_028096.1:g.40788C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*58C>T MANE Select ENSP00000263063.3:n.*58C>T
ENST00000263063.8:c.*58C>T ENSP00000263063.3:n.*58C>T
ENST00000488290.5:n.3562C>T
NM_018109.3:c.*58C>T NP_060579.3:n.*58C>T
NM_018109.4:c.*58C>T MANE Select NP_060579.3:n.*58C>T
Search 100 bp 5'
Search 100 bp 3'