Canonical Allele Identifier: CA421405175

Gene: MPZ

Linked Data

• MyVariant Identifiers: chr1:g.161276604T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161306814T>G , CM000663.2:g.161306814T>G	GRCh38
NC_000001.10:g.161276604T>G , CM000663.1:g.161276604T>G	GRCh37
NC_000001.9:g.159543228T>G	NCBI36
NG_008055.1:g.8159A>C , LRG_256:g.8159A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.342A>C	ENSP00000488104.2:p.Ile114=
ENST00000533357.5:c.342A>C MANE Select	ENSP00000432943.1:p.Ile114=
ENST00000672287.2:c.-247A>C	ENSP00000499818.2:n.-247A>C
ENST00000672602.2:c.342A>C	ENSP00000500814.2:p.Ile114=
ENST00000674861.1:n.405A>C
ENST00000463290.5:c.342A>C	ENSP00000431538.1:p.Ile114=
ENST00000491222.5:c.-247A>C	ENSP00000431441.1:n.-247A>C
ENST00000526189.2:c.86A>C
ENST00000533357.4:c.342A>C	ENSP00000432943.1:p.Ile114=
NM_000530.6:c.342A>C , LRG_256t1:c.342A>C	NP_000521.2:p.Ile114=
NM_000530.7:c.342A>C	NP_000521.2:p.Ile114=
NM_001315491.1:c.342A>C	NP_001302420.1:p.Ile114=
XM_017001321.2:c.372A>C	XP_016856810.1:p.Ile124=
NM_000530.8:c.342A>C MANE Select	NP_000521.2:p.Ile114=
NM_001315491.2:c.342A>C	NP_001302420.1:p.Ile114=