Canonical Allele Identifier: CA526974627

Gene: MPZL1

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

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

Transcript Alleles

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