Canonical Allele Identifier: CA1202691013
Gene: MPZ HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161307419A= , CM000663.2:g.161307419A= GRCh38
NC_000001.10:g.161277209A= , CM000663.1:g.161277209A= GRCh37
NC_000001.9:g.159543833A= NCBI36
NG_008055.1:g.7554T= , LRG_256:g.7554T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000526189.3:c.73T= ENSP00000488104.2:p.Ser25=
ENST00000533357.5:c.73T= MANE Select ENSP00000432943.1:p.Ser25=
ENST00000672287.2:c.-516T= ENSP00000499818.2:n.-516T=
ENST00000672602.2:c.73T= ENSP00000500814.2:p.Ser25=
ENST00000674861.1:n.136T=
ENST00000463290.5:c.73T= ENSP00000431538.1:p.Ser25=
ENST00000491222.5:c.-516T= ENSP00000431441.1:n.-516T=
ENST00000533357.4:c.73T= ENSP00000432943.1:p.Ser25=
NM_000530.6:c.73T= , LRG_256t1:c.73T= NP_000521.2:p.Ser25=
NM_000530.7:c.73T= NP_000521.2:p.Ser25=
NM_001315491.1:c.73T= NP_001302420.1:p.Ser25=
XM_017001321.2:c.103T= XP_016856810.1:p.Ser35=
NM_000530.8:c.73T= MANE Select NP_000521.2:p.Ser25=
NM_001315491.2:c.73T= NP_001302420.1:p.Ser25=