Canonical Allele Identifier: CA392606914

Gene: MYZAP GCOM1

Linked Data

• MyVariant Identifiers: chr15:g.57910304C>G (hg19) ; chr15:g.57618106C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.57618106C>G , CM000677.2:g.57618106C>G	GRCh38
NC_000015.9:g.57910304C>G , CM000677.1:g.57910304C>G	GRCh37
NC_000015.8:g.55697596C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267853.10:c.236C>G (MYZAP) MANE Select	ENSP00000267853.5:p.Ser79Ter
ENST00000649429.1:c.236C>G (GCOM1)	ENSP00000497390.1:p.Ser79Ter
ENST00000267853.9:c.236C>G (MYZAP)	ENSP00000267853.5:p.Ser79Ter
ENST00000380565.8:c.236C>G (MYZAP)	ENSP00000369939.4:p.Ser79Ter
ENST00000380568.7:c.236C>G (GCOM1)	ENSP00000369942.3:p.Ser79Ter
ENST00000380569.6:c.236C>G (GCOM1)	ENSP00000369943.2:p.Ser79Ter
ENST00000460962.5:c.236C>G (GCOM1)	ENSP00000435774.1:p.Ser79Ter
ENST00000463717.5:c.236C>G (GCOM1)	ENSP00000435028.1:p.Ser79Ter
ENST00000468886.5:c.236C>G (GCOM1)	ENSP00000433702.1:p.Ser79Ter
ENST00000471563.5:c.236C>G (GCOM1)	ENSP00000432563.1:p.Ser79Ter
ENST00000477282.5:c.236C>G (GCOM1)	ENSP00000434505.1:p.Ser79Ter
ENST00000482814.5:c.236C>G (GCOM1)	ENSP00000436922.1:p.Ser79Ter
ENST00000488175.5:c.236C>G (GCOM1)	ENSP00000432066.1:p.Ser79Ter
ENST00000496101.5:c.236C>G (GCOM1)	ENSP00000434588.1:p.Ser79Ter
ENST00000496627.5:c.236C>G (GCOM1)	ENSP00000436614.1:p.Ser79Ter
ENST00000569089.1:c.191C>G (MYZAP)	ENSP00000457126.1:p.Ser64Ter
ENST00000587652.5:c.236C>G (GCOM1)	ENSP00000465231.1:p.Ser79Ter
NM_001018090.6:c.236C>G (GCOM1)	NP_001018100.1:p.Ser79Ter
NM_001018091.6:c.236C>G (GCOM1)	NP_001018101.1:p.Ser79Ter
NM_001018100.4:c.236C>G (MYZAP)	NP_001018110.1:p.Ser79Ter
NM_001285900.3:c.236C>G (GCOM1)	NP_001272829.1:p.Ser79Ter
NM_152451.7:c.236C>G (MYZAP)	NP_689664.3:p.Ser79Ter
NR_104367.2:n.367C>G (GCOM1)
NR_104368.2:n.367C>G (GCOM1)
NR_104369.2:n.367C>G (GCOM1)
NR_104370.2:n.367C>G (GCOM1)
NR_104371.3:n.367C>G (GCOM1)
NM_001018100.5:c.236C>G (MYZAP) MANE Select	NP_001018110.1:p.Ser79Ter
NM_152451.8:c.236C>G (MYZAP)	NP_689664.3:p.Ser79Ter