Canonical Allele Identifier: CA2207124507

Gene: EMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10539262_10539266delinsTTTCC , CM000678.2:g.10539262_10539266delinsTTTCC	GRCh38
NC_000016.9:g.10633119_10633123delinsTTTCC , CM000678.1:g.10633119_10633123delinsTTTCC	GRCh37
NC_000016.8:g.10540620_10540624delinsTTTCC	NCBI36
NG_042058.1:g.46451_46455delinsGGAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359543.8:c.170-1192_170-1188delinsGGAAA MANE Select	ENSP00000352540.3:n.170-1192_170-1188delinsGGAAA
ENST00000359543.7:c.170-1192_170-1188delinsGGAAA	ENSP00000352540.3:n.170-1192_170-1188delinsGGAAA
ENST00000536829.1:c.170-1192_170-1188delinsGGAAA	ENSP00000445712.1:n.170-1192_170-1188delinsGGAAA
NM_001424.4:c.170-1192_170-1188delinsGGAAA	NP_001415.1:n.170-1192_170-1188delinsGGAAA
NM_001424.5:c.170-1192_170-1188delinsGGAAA	NP_001415.1:n.170-1192_170-1188delinsGGAAA
XM_006720864.2:c.170-1192_170-1188delinsGGAAA	XP_006720927.1:n.170-1192_170-1188delinsGGAAA
XM_006720864.3:c.170-1192_170-1188delinsGGAAA	XP_006720927.1:n.170-1192_170-1188delinsGGAAA
NM_001424.6:c.170-1192_170-1188delinsGGAAA MANE Select	NP_001415.1:n.170-1192_170-1188delinsGGAAA