Canonical Allele Identifier: CA2586967672

Gene: MPZ

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.161307321_161307341del , CM000663.2:g.161307321_161307341del	GRCh38
NC_000001.10:g.161277111_161277131del , CM000663.1:g.161277111_161277131del	GRCh37
NC_000001.9:g.159543735_159543755del	NCBI36
NG_008055.1:g.7632_7652del , LRG_256:g.7632_7652del

Transcript Alleles

HGVS	Amino-acid change
ENST00000526189.3:c.151_171del	ENSP00000488104.2:p.Ser51_Trp57del
ENST00000533357.5:c.151_171del MANE Select	ENSP00000432943.1:p.Ser51_Trp57del
ENST00000672287.2:c.-438_-418del	ENSP00000499818.2:n.-438_-418del
ENST00000672602.2:c.151_171del	ENSP00000500814.2:p.Ser51_Trp57del
ENST00000674861.1:n.214_234del
ENST00000463290.5:c.151_171del	ENSP00000431538.1:p.Ser51_Trp57del
ENST00000491222.5:c.-438_-418del	ENSP00000431441.1:n.-438_-418del
ENST00000533357.4:c.151_171del	ENSP00000432943.1:p.Ser51_Trp57del
NM_000530.6:c.151_171del , LRG_256t1:c.151_171del	NP_000521.2:p.Ser51_Trp57del
NM_000530.7:c.151_171del	NP_000521.2:p.Ser51_Trp57del
NM_001315491.1:c.151_171del	NP_001302420.1:p.Ser51_Trp57del
XM_017001321.2:c.181_201del	XP_016856810.1:p.Ser61_Trp67del
NM_000530.8:c.151_171del MANE Select	NP_000521.2:p.Ser51_Trp57del
NM_001315491.2:c.151_171del	NP_001302420.1:p.Ser51_Trp57del