Canonical Allele Identifier: CA1143531511

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306116C= , CM000663.2:g.161306116C=	GRCh38
NC_000001.10:g.161275906C= , CM000663.1:g.161275906C=	GRCh37
NC_000001.9:g.159542530C=	NCBI36
NG_008055.1:g.8857G= , LRG_256:g.8857G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.556G=	ENSP00000488104.2:p.Gly186=
ENST00000533357.5:c.637G= MANE Select	ENSP00000432943.1:p.Gly213=
ENST00000672287.2:c.49G=	ENSP00000499818.2:p.Gly17=
ENST00000672602.2:c.637G=	ENSP00000500814.2:p.Gly213=
ENST00000674861.1:n.700G=
ENST00000463290.5:c.637G=	ENSP00000431538.1:p.Gly213=
ENST00000476410.1:n.97G=
ENST00000488271.1:n.75G=
ENST00000491222.5:c.49G=	ENSP00000431441.1:p.Gly17=
ENST00000526189.2:c.300G=
ENST00000533357.4:c.637G=	ENSP00000432943.1:p.Gly213=
NM_000530.6:c.637G= , LRG_256t1:c.637G=	NP_000521.2:p.Gly213=
NM_000530.7:c.637G=	NP_000521.2:p.Gly213=
NM_001315491.1:c.637G=	NP_001302420.1:p.Gly213=
XM_017001321.2:c.667G=	XP_016856810.1:p.Gly223=
NM_000530.8:c.637G= MANE Select	NP_000521.2:p.Gly213=
NM_001315491.2:c.637G=	NP_001302420.1:p.Gly213=