Canonical Allele Identifier: CA2207124337

Gene: EMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10538983_10538984delinsAT , CM000678.2:g.10538983_10538984delinsAT	GRCh38
NC_000016.9:g.10632840_10632841delinsAT , CM000678.1:g.10632840_10632841delinsAT	GRCh37
NC_000016.8:g.10540341_10540342delinsAT	NCBI36
NG_042058.1:g.46733_46734delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359543.8:c.170-910_170-909delinsAT MANE Select	ENSP00000352540.3:n.170-910_170-909delinsAT
ENST00000359543.7:c.170-910_170-909delinsAT	ENSP00000352540.3:n.170-910_170-909delinsAT
ENST00000536829.1:c.170-910_170-909delinsAT	ENSP00000445712.1:n.170-910_170-909delinsAT
NM_001424.4:c.170-910_170-909delinsAT	NP_001415.1:n.170-910_170-909delinsAT
NM_001424.5:c.170-910_170-909delinsAT	NP_001415.1:n.170-910_170-909delinsAT
XM_006720864.2:c.170-910_170-909delinsAT	XP_006720927.1:n.170-910_170-909delinsAT
XM_006720864.3:c.170-910_170-909delinsAT	XP_006720927.1:n.170-910_170-909delinsAT
NM_001424.6:c.170-910_170-909delinsAT MANE Select	NP_001415.1:n.170-910_170-909delinsAT