Canonical Allele Identifier: CA1202690422

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161307244C= , CM000663.2:g.161307244C=	GRCh38
NC_000001.10:g.161277034C= , CM000663.1:g.161277034C=	GRCh37
NC_000001.9:g.159543658C=	NCBI36
NG_008055.1:g.7729G= , LRG_256:g.7729G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000526189.3:c.234+14G=	ENSP00000488104.2:n.234+14G=
ENST00000533357.5:c.234+14G= MANE Select	ENSP00000432943.1:n.234+14G=
ENST00000672287.2:c.-355+14G=	ENSP00000499818.2:n.-355+14G=
ENST00000672602.2:c.234+14G=	ENSP00000500814.2:n.234+14G=
ENST00000674861.1:n.297+14G=
ENST00000463290.5:c.234+14G=	ENSP00000431538.1:n.234+14G=
ENST00000491222.5:c.-355+14G=	ENSP00000431441.1:n.-355+14G=
ENST00000533357.4:c.234+14G=	ENSP00000432943.1:n.234+14G=
NM_000530.6:c.234+14G= , LRG_256t1:c.234+14G=	NP_000521.2:n.234+14G=
NM_000530.7:c.234+14G=	NP_000521.2:n.234+14G=
NM_001315491.1:c.234+14G=	NP_001302420.1:n.234+14G=
XM_017001321.2:c.264+14G=	XP_016856810.1:n.264+14G=
NM_000530.8:c.234+14G= MANE Select	NP_000521.2:n.234+14G=
NM_001315491.2:c.234+14G=	NP_001302420.1:n.234+14G=