Canonical Allele Identifier: CA2207124456

Gene: EMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10539214_10539215delinsAG , CM000678.2:g.10539214_10539215delinsAG	GRCh38
NC_000016.9:g.10633071_10633072delinsAG , CM000678.1:g.10633071_10633072delinsAG	GRCh37
NC_000016.8:g.10540572_10540573delinsAG	NCBI36
NG_042058.1:g.46502_46503delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359543.8:c.170-1141_170-1140delinsCT MANE Select	ENSP00000352540.3:n.170-1141_170-1140delinsCT
ENST00000359543.7:c.170-1141_170-1140delinsCT	ENSP00000352540.3:n.170-1141_170-1140delinsCT
ENST00000536829.1:c.170-1141_170-1140delinsCT	ENSP00000445712.1:n.170-1141_170-1140delinsCT
NM_001424.4:c.170-1141_170-1140delinsCT	NP_001415.1:n.170-1141_170-1140delinsCT
NM_001424.5:c.170-1141_170-1140delinsCT	NP_001415.1:n.170-1141_170-1140delinsCT
XM_006720864.2:c.170-1141_170-1140delinsCT	XP_006720927.1:n.170-1141_170-1140delinsCT
XM_006720864.3:c.170-1141_170-1140delinsCT	XP_006720927.1:n.170-1141_170-1140delinsCT
NM_001424.6:c.170-1141_170-1140delinsCT MANE Select	NP_001415.1:n.170-1141_170-1140delinsCT