Canonical Allele Identifier: CA2540783279

Gene: EMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10538959_10538960insTGTGTGCCACCACACC , CM000678.2:g.10538959_10538960insTGTGTGCCACCACACC	GRCh38
NC_000016.9:g.10632816_10632817insTGTGTGCCACCACACC , CM000678.1:g.10632816_10632817insTGTGTGCCACCACACC	GRCh37
NC_000016.8:g.10540317_10540318insTGTGTGCCACCACACC	NCBI36
NG_042058.1:g.46757_46758insGGTGTGGTGGCACACA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359543.8:c.170-886_170-885insGGTGTGGTGGCACACA MANE Select	ENSP00000352540.3:n.170-886_170-885insGGTGTGGTGGCACACA
ENST00000359543.7:c.170-886_170-885insGGTGTGGTGGCACACA	ENSP00000352540.3:n.170-886_170-885insGGTGTGGTGGCACACA
ENST00000536829.1:c.170-886_170-885insGGTGTGGTGGCACACA	ENSP00000445712.1:n.170-886_170-885insGGTGTGGTGGCACACA
NM_001424.4:c.170-886_170-885insGGTGTGGTGGCACACA	NP_001415.1:n.170-886_170-885insGGTGTGGTGGCACACA
NM_001424.5:c.170-886_170-885insGGTGTGGTGGCACACA	NP_001415.1:n.170-886_170-885insGGTGTGGTGGCACACA
XM_006720864.2:c.170-886_170-885insGGTGTGGTGGCACACA	XP_006720927.1:n.170-886_170-885insGGTGTGGTGGCACACA
XM_006720864.3:c.170-886_170-885insGGTGTGGTGGCACACA	XP_006720927.1:n.170-886_170-885insGGTGTGGTGGCACACA
NM_001424.6:c.170-886_170-885insGGTGTGGTGGCACACA MANE Select	NP_001415.1:n.170-886_170-885insGGTGTGGTGGCACACA