Canonical Allele Identifier: CA2207124479

Gene: EMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10539242_10539243delinsCT , CM000678.2:g.10539242_10539243delinsCT	GRCh38
NC_000016.9:g.10633099_10633100delinsCT , CM000678.1:g.10633099_10633100delinsCT	GRCh37
NC_000016.8:g.10540600_10540601delinsCT	NCBI36
NG_042058.1:g.46474_46475delinsAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359543.8:c.170-1169_170-1168delinsAG MANE Select	ENSP00000352540.3:n.170-1169_170-1168delinsAG
ENST00000359543.7:c.170-1169_170-1168delinsAG	ENSP00000352540.3:n.170-1169_170-1168delinsAG
ENST00000536829.1:c.170-1169_170-1168delinsAG	ENSP00000445712.1:n.170-1169_170-1168delinsAG
NM_001424.4:c.170-1169_170-1168delinsAG	NP_001415.1:n.170-1169_170-1168delinsAG
NM_001424.5:c.170-1169_170-1168delinsAG	NP_001415.1:n.170-1169_170-1168delinsAG
XM_006720864.2:c.170-1169_170-1168delinsAG	XP_006720927.1:n.170-1169_170-1168delinsAG
XM_006720864.3:c.170-1169_170-1168delinsAG	XP_006720927.1:n.170-1169_170-1168delinsAG
NM_001424.6:c.170-1169_170-1168delinsAG MANE Select	NP_001415.1:n.170-1169_170-1168delinsAG