Canonical Allele Identifier: CA376434173
Gene: MTPAP HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.30602655C>G (hg19) chr10:g.30313726C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313726C>G , CM000672.2:g.30313726C>G GRCh38
NC_000010.10:g.30602655C>G , CM000672.1:g.30602655C>G GRCh37
NC_000010.9:g.30642661C>G NCBI36
NG_028096.1:g.40613G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1632G>C MANE Select ENSP00000263063.3:p.Lys544Asn
ENST00000263063.8:c.1632G>C ENSP00000263063.3:p.Lys544Asn
ENST00000488290.5:n.3387G>C
NM_018109.3:c.1632G>C NP_060579.3:p.Lys544Asn
NM_018109.4:c.1632G>C MANE Select NP_060579.3:p.Lys544Asn
Search 100 bp 5'
Search 100 bp 3'