Canonical Allele Identifier: CA343353400
Community Standard Title: NM_000530.8(MPZ):c.1A>G (p.Met1Val)
Gene: MPZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161309905T>C , CM000663.2:g.161309905T>C GRCh38
NC_000001.10:g.161279695T>C , CM000663.1:g.161279695T>C GRCh37
NC_000001.9:g.159546319T>C NCBI36
NG_008055.1:g.5068A>G , LRG_256:g.5068A>G
NG_012767.1:g.530T>C , LRG_317:g.530T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000530.8:c.1A>G MANE Select NP_000521.2:p.Met1Val
ENST00000533357.5:c.1A>G MANE Select ENSP00000432943.1:p.Met1Val
NM_000530.6:c.1A>G , LRG_256t1:c.1A>G NP_000521.2:p.Met1Val
NM_000530.7:c.1A>G NP_000521.2:p.Met1Val
NM_001315491.1:c.1A>G NP_001302420.1:p.Met1Val
NM_001315491.2:c.1A>G NP_001302420.1:p.Met1Val
ENST00000463290.5:c.1A>G ENSP00000431538.1:p.Met1Val
ENST00000526189.3:c.1A>G ENSP00000488104.2:p.Met1Val
ENST00000533357.4:c.1A>G ENSP00000432943.1:p.Met1Val
ENST00000672602.2:c.1A>G ENSP00000500814.2:p.Met1Val
ENST00000674861.1:n.64A>G
XM_017001321.2:c.31A>G XP_016856810.1:p.Met11Val