Canonical Allele Identifier: CA663650004
Gene: MTPAP HGNC NCBI

Linked Data

dbSNP Id: rs1421777301

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313489T>C , CM000672.2:g.30313489T>C GRCh38
NC_000010.10:g.30602418T>C , CM000672.1:g.30602418T>C GRCh37
NC_000010.9:g.30642424T>C NCBI36
NG_028096.1:g.40850A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.*120A>G MANE Select ENSP00000263063.3:n.*120A>G
ENST00000263063.8:c.*120A>G ENSP00000263063.3:n.*120A>G
ENST00000488290.5:n.3624A>G
NM_018109.3:c.*120A>G NP_060579.3:n.*120A>G
NM_018109.4:c.*120A>G MANE Select NP_060579.3:n.*120A>G