Canonical Allele Identifier: CA229484685

Gene: MPZL3

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.118246303G>T , CM000673.2:g.118246303G>T	GRCh38
NC_000011.9:g.118117018G>T , CM000673.1:g.118117018G>T	GRCh37
NC_000011.8:g.117622228G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000278949.9:c.73+5919C>A MANE Select	ENSP00000278949.4:n.73+5919C>A
ENST00000278949.8:c.73+5919C>A	ENSP00000278949.4:n.73+5919C>A
ENST00000446386.2:c.73+5919C>A	ENSP00000393594.2:n.73+5919C>A
ENST00000525386.5:c.73+5919C>A	ENSP00000434636.1:n.73+5919C>A
ENST00000527472.1:c.73+5919C>A	ENSP00000432106.1:n.73+5919C>A
NM_001286152.1:c.73+5919C>A	NP_001273081.1:n.73+5919C>A
NM_198275.2:c.73+5919C>A	NP_938016.1:n.73+5919C>A
NR_104404.1:n.147+5919C>A
NR_104405.1:n.147+5919C>A
XR_947802.1:n.99+5919C>A
NM_198275.3:c.73+5919C>A MANE Select	NP_938016.1:n.73+5919C>A
NM_001286152.2:c.73+5919C>A	NP_001273081.1:n.73+5919C>A
NR_104404.2:n.144+5919C>A
NR_104405.2:n.144+5919C>A