Canonical Allele Identifier: CA334216
Gene: MPZ HGNC NCBI

Linked Data

ClinVar Variation Id: 188168
ClinVar RCV Id: RCV000168067 RCV000236489 RCV000790119
dbSNP Id: rs786204119
MyVariant Identifiers: chr1:g.161277100T>C (hg19) chr1:g.161307310T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161307310T>C , CM000663.2:g.161307310T>C GRCh38
NC_000001.10:g.161277100T>C , CM000663.1:g.161277100T>C GRCh37
NC_000001.9:g.159543724T>C NCBI36
NG_008055.1:g.7663A>G , LRG_256:g.7663A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000526189.3:c.182A>G ENSP00000488104.2:p.Asp61Gly
ENST00000533357.5:c.182A>G MANE Select ENSP00000432943.1:p.Asp61Gly
ENST00000672287.2:c.-407A>G ENSP00000499818.2:n.-407A>G
ENST00000672602.2:c.182A>G ENSP00000500814.2:p.Asp61Gly
ENST00000674861.1:n.245A>G
ENST00000463290.5:c.182A>G ENSP00000431538.1:p.Asp61Gly
ENST00000491222.5:c.-407A>G ENSP00000431441.1:n.-407A>G
ENST00000533357.4:c.182A>G ENSP00000432943.1:p.Asp61Gly
NM_000530.6:c.182A>G , LRG_256t1:c.182A>G NP_000521.2:p.Asp61Gly
NM_000530.7:c.182A>G NP_000521.2:p.Asp61Gly
NM_001315491.1:c.182A>G NP_001302420.1:p.Asp61Gly
XM_017001321.2:c.212A>G XP_016856810.1:p.Asp71Gly
NM_000530.8:c.182A>G MANE Select NP_000521.2:p.Asp61Gly
NM_001315491.2:c.182A>G NP_001302420.1:p.Asp61Gly
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