Canonical Allele Identifier: CA376433774
Gene: MTPAP HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.30602562C>A (hg19) chr10:g.30313633C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.30313633C>A , CM000672.2:g.30313633C>A GRCh38
NC_000010.10:g.30602562C>A , CM000672.1:g.30602562C>A GRCh37
NC_000010.9:g.30642568C>A NCBI36
NG_028096.1:g.40706G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263063.9:c.1725G>T MANE Select ENSP00000263063.3:p.Lys575Asn
ENST00000263063.8:c.1725G>T ENSP00000263063.3:p.Lys575Asn
ENST00000488290.5:n.3480G>T
NM_018109.3:c.1725G>T NP_060579.3:p.Lys575Asn
NM_018109.4:c.1725G>T MANE Select NP_060579.3:p.Lys575Asn
Search 100 bp 5'
Search 100 bp 3'