Canonical Allele Identifier: CA1143538429
Gene: MPZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161306767T= , CM000663.2:g.161306767T= GRCh38
NC_000001.10:g.161276557T= , CM000663.1:g.161276557T= GRCh37
NC_000001.9:g.159543181T= NCBI36
NG_008055.1:g.8206A= , LRG_256:g.8206A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000526189.3:c.367+22A= ENSP00000488104.2:n.367+22A=
ENST00000533357.5:c.389A= MANE Select ENSP00000432943.1:p.Lys130=
ENST00000672287.2:c.-200A= ENSP00000499818.2:n.-200A=
ENST00000672602.2:c.389A= ENSP00000500814.2:p.Lys130=
ENST00000674861.1:n.452A=
ENST00000463290.5:c.389A= ENSP00000431538.1:p.Lys130=
ENST00000491222.5:c.-200A= ENSP00000431441.1:n.-200A=
ENST00000526189.2:c.111+22A=
ENST00000533357.4:c.389A= ENSP00000432943.1:p.Lys130=
NM_000530.6:c.389A= , LRG_256t1:c.389A= NP_000521.2:p.Lys130=
NM_000530.7:c.389A= NP_000521.2:p.Lys130=
NM_001315491.1:c.389A= NP_001302420.1:p.Lys130=
XM_017001321.2:c.419A= XP_016856810.1:p.Lys140=
NM_000530.8:c.389A= MANE Select NP_000521.2:p.Lys130=
NM_001315491.2:c.389A= NP_001302420.1:p.Lys130=