Canonical Allele Identifier: CA343351543

Gene: MPZ

Linked Data

• ClinVar Variation Id: 637323
• ClinVar RCV Id: RCV000789435 ; RCV002249492 ; RCV003581718
• dbSNP Id: rs1571820317
• MyVariant Identifiers: chr1:g.161277181G>A (hg19) ; chr1:g.161307391G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161307391G>A , CM000663.2:g.161307391G>A	GRCh38
NC_000001.10:g.161277181G>A , CM000663.1:g.161277181G>A	GRCh37
NC_000001.9:g.159543805G>A	NCBI36
NG_008055.1:g.7582C>T , LRG_256:g.7582C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.101C>T	ENSP00000488104.2:p.Thr34Ile
ENST00000533357.5:c.101C>T MANE Select	ENSP00000432943.1:p.Thr34Ile
ENST00000672287.2:c.-488C>T	ENSP00000499818.2:n.-488C>T
ENST00000672602.2:c.101C>T	ENSP00000500814.2:p.Thr34Ile
ENST00000674861.1:n.164C>T
ENST00000463290.5:c.101C>T	ENSP00000431538.1:p.Thr34Ile
ENST00000491222.5:c.-488C>T	ENSP00000431441.1:n.-488C>T
ENST00000533357.4:c.101C>T	ENSP00000432943.1:p.Thr34Ile
NM_000530.6:c.101C>T , LRG_256t1:c.101C>T	NP_000521.2:p.Thr34Ile
NM_000530.7:c.101C>T	NP_000521.2:p.Thr34Ile
NM_001315491.1:c.101C>T	NP_001302420.1:p.Thr34Ile
XM_017001321.2:c.131C>T	XP_016856810.1:p.Thr44Ile
NM_000530.8:c.101C>T MANE Select	NP_000521.2:p.Thr34Ile
NM_001315491.2:c.101C>T	NP_001302420.1:p.Thr34Ile