Canonical Allele Identifier: CA421405223

Gene: MPZ

Linked Data

• MyVariant Identifiers: chr1:g.161276631A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306841A>T , CM000663.2:g.161306841A>T	GRCh38
NC_000001.10:g.161276631A>T , CM000663.1:g.161276631A>T	GRCh37
NC_000001.9:g.159543255A>T	NCBI36
NG_008055.1:g.8132T>A , LRG_256:g.8132T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.315T>A	ENSP00000488104.2:p.Pro105=
ENST00000533357.5:c.315T>A MANE Select	ENSP00000432943.1:p.Pro105=
ENST00000672287.2:c.-274T>A	ENSP00000499818.2:n.-274T>A
ENST00000672602.2:c.315T>A	ENSP00000500814.2:p.Pro105=
ENST00000674861.1:n.378T>A
ENST00000463290.5:c.315T>A	ENSP00000431538.1:p.Pro105=
ENST00000491222.5:c.-274T>A	ENSP00000431441.1:n.-274T>A
ENST00000526189.2:c.59T>A
ENST00000533357.4:c.315T>A	ENSP00000432943.1:p.Pro105=
NM_000530.6:c.315T>A , LRG_256t1:c.315T>A	NP_000521.2:p.Pro105=
NM_000530.7:c.315T>A	NP_000521.2:p.Pro105=
NM_001315491.1:c.315T>A	NP_001302420.1:p.Pro105=
XM_017001321.2:c.345T>A	XP_016856810.1:p.Pro115=
NM_000530.8:c.315T>A MANE Select	NP_000521.2:p.Pro105=
NM_001315491.2:c.315T>A	NP_001302420.1:p.Pro105=