Canonical Allele Identifier: CA421405182

Gene: MPZ

Linked Data

• MyVariant Identifiers: chr1:g.161276607G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306817G>C , CM000663.2:g.161306817G>C	GRCh38
NC_000001.10:g.161276607G>C , CM000663.1:g.161276607G>C	GRCh37
NC_000001.9:g.159543231G>C	NCBI36
NG_008055.1:g.8156C>G , LRG_256:g.8156C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000526189.3:c.339C>G	ENSP00000488104.2:p.Val113=
ENST00000533357.5:c.339C>G MANE Select	ENSP00000432943.1:p.Val113=
ENST00000672287.2:c.-250C>G	ENSP00000499818.2:n.-250C>G
ENST00000672602.2:c.339C>G	ENSP00000500814.2:p.Val113=
ENST00000674861.1:n.402C>G
ENST00000463290.5:c.339C>G	ENSP00000431538.1:p.Val113=
ENST00000491222.5:c.-250C>G	ENSP00000431441.1:n.-250C>G
ENST00000526189.2:c.83C>G
ENST00000533357.4:c.339C>G	ENSP00000432943.1:p.Val113=
NM_000530.6:c.339C>G , LRG_256t1:c.339C>G	NP_000521.2:p.Val113=
NM_000530.7:c.339C>G	NP_000521.2:p.Val113=
NM_001315491.1:c.339C>G	NP_001302420.1:p.Val113=
XM_017001321.2:c.369C>G	XP_016856810.1:p.Val123=
NM_000530.8:c.339C>G MANE Select	NP_000521.2:p.Val113=
NM_001315491.2:c.339C>G	NP_001302420.1:p.Val113=