Canonical Allele Identifier: CA1143538440

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306915G= , CM000663.2:g.161306915G=	GRCh38
NC_000001.10:g.161276705G= , CM000663.1:g.161276705G=	GRCh37
NC_000001.9:g.159543329G=	NCBI36
NG_008055.1:g.8058C= , LRG_256:g.8058C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.241C=	ENSP00000488104.2:p.His81=
ENST00000533357.5:c.241C= MANE Select	ENSP00000432943.1:p.His81=
ENST00000672287.2:c.-348C=	ENSP00000499818.2:n.-348C=
ENST00000672602.2:c.241C=	ENSP00000500814.2:p.His81=
ENST00000674861.1:n.304C=
ENST00000463290.5:c.241C=	ENSP00000431538.1:p.His81=
ENST00000491222.5:c.-348C=	ENSP00000431441.1:n.-348C=
ENST00000533357.4:c.241C=	ENSP00000432943.1:p.His81=
NM_000530.6:c.241C= , LRG_256t1:c.241C=	NP_000521.2:p.His81=
NM_000530.7:c.241C=	NP_000521.2:p.His81=
NM_001315491.1:c.241C=	NP_001302420.1:p.His81=
XM_017001321.2:c.271C=	XP_016856810.1:p.His91=
NM_000530.8:c.241C= MANE Select	NP_000521.2:p.His81=
NM_001315491.2:c.241C=	NP_001302420.1:p.His81=