Canonical Allele Identifier: CA343349708
Gene: MPZ HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.161306876T>C , CM000663.2:g.161306876T>C GRCh38
NC_000001.10:g.161276666T>C , CM000663.1:g.161276666T>C GRCh37
NC_000001.9:g.159543290T>C NCBI36
NG_008055.1:g.8097A>G , LRG_256:g.8097A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000526189.3:c.280A>G ENSP00000488104.2:p.Thr94Ala
ENST00000533357.5:c.280A>G MANE Select ENSP00000432943.1:p.Thr94Ala
ENST00000672287.2:c.-309A>G ENSP00000499818.2:n.-309A>G
ENST00000672602.2:c.280A>G ENSP00000500814.2:p.Thr94Ala
ENST00000674861.1:n.343A>G
ENST00000463290.5:c.280A>G ENSP00000431538.1:p.Thr94Ala
ENST00000491222.5:c.-309A>G ENSP00000431441.1:n.-309A>G
ENST00000526189.2:c.24A>G
ENST00000533357.4:c.280A>G ENSP00000432943.1:p.Thr94Ala
NM_000530.6:c.280A>G , LRG_256t1:c.280A>G NP_000521.2:p.Thr94Ala
NM_000530.7:c.280A>G NP_000521.2:p.Thr94Ala
NM_001315491.1:c.280A>G NP_001302420.1:p.Thr94Ala
XM_017001321.2:c.310A>G XP_016856810.1:p.Thr104Ala
NM_000530.8:c.280A>G MANE Select NP_000521.2:p.Thr94Ala
NM_001315491.2:c.280A>G NP_001302420.1:p.Thr94Ala