Canonical Allele Identifier: CA343344445

Gene: MPZ

Linked Data

• dbSNP Id: rs1670227174
• MyVariant Identifiers: chr1:g.161275757A>G (hg19) ; chr1:g.161305967A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161305967A>G , CM000663.2:g.161305967A>G	GRCh38
NC_000001.10:g.161275757A>G , CM000663.1:g.161275757A>G	GRCh37
NC_000001.9:g.159542381A>G	NCBI36
NG_008055.1:g.9006T>C , LRG_256:g.9006T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000526189.3:c.575T>C	ENSP00000488104.2:p.Leu192Pro
ENST00000533357.5:c.656T>C MANE Select	ENSP00000432943.1:p.Leu219Pro
ENST00000672287.2:c.68T>C	ENSP00000499818.2:p.Leu23Pro
ENST00000672602.2:c.656T>C	ENSP00000500814.2:p.Leu219Pro
ENST00000674861.1:n.719T>C
ENST00000463290.5:c.656T>C	ENSP00000431538.1:p.Leu219Pro
ENST00000476410.1:n.246T>C
ENST00000488271.1:n.94T>C
ENST00000491222.5:c.68T>C	ENSP00000431441.1:p.Leu23Pro
ENST00000526189.2:c.319T>C
ENST00000533357.4:c.656T>C	ENSP00000432943.1:p.Leu219Pro
NM_000530.6:c.656T>C , LRG_256t1:c.656T>C	NP_000521.2:p.Leu219Pro
NM_000530.7:c.656T>C	NP_000521.2:p.Leu219Pro
NM_001315491.1:c.656T>C	NP_001302420.1:p.Leu219Pro
XM_017001321.2:c.675+141T>C	XP_016856810.1:n.675+141T>C
NM_000530.8:c.656T>C MANE Select	NP_000521.2:p.Leu219Pro
NM_001315491.2:c.656T>C	NP_001302420.1:p.Leu219Pro