Canonical Allele Identifier: CA31993372
Community Standard Title: NM_003953.6(MPZL1):c.92-16321A>G
Gene: MPZL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.167749262A>G , CM000663.2:g.167749262A>G GRCh38
NC_000001.10:g.167718499A>G , CM000663.1:g.167718499A>G GRCh37
NC_000001.9:g.165985123A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_003953.6:c.92-16321A>G MANE Select NP_003944.1:n.92-16321A>G
ENST00000359523.7:c.92-16321A>G MANE Select ENSP00000352513.2:n.92-16321A>G
NM_001146191.1:c.92-16321A>G NP_001139663.1:n.92-16321A>G
NM_001146191.2:c.92-16321A>G NP_001139663.1:n.92-16321A>G
NM_003953.5:c.92-16321A>G NP_003944.1:n.92-16321A>G
NM_024569.4:c.92-16321A>G NP_078845.3:n.92-16321A>G
NM_024569.5:c.92-16321A>G NP_078845.3:n.92-16321A>G
ENST00000359523.6:c.92-16321A>G ENSP00000352513.2:n.92-16321A>G
ENST00000392121.7:c.92-16321A>G ENSP00000375968.3:n.92-16321A>G
ENST00000448405.5:c.92-16321A>G ENSP00000399490.1:n.92-16321A>G
ENST00000464954.1:n.294-16321A>G
ENST00000465787.5:n.251-16321A>G
ENST00000474859.5:c.92-16321A>G ENSP00000420455.1:n.92-16321A>G