Canonical Allele Identifier: CA2207124480

Gene: EMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10539244_10539248delinsTTTTC , CM000678.2:g.10539244_10539248delinsTTTTC	GRCh38
NC_000016.9:g.10633101_10633105delinsTTTTC , CM000678.1:g.10633101_10633105delinsTTTTC	GRCh37
NC_000016.8:g.10540602_10540606delinsTTTTC	NCBI36
NG_042058.1:g.46469_46473delinsGAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359543.8:c.170-1174_170-1170delinsGAAAA MANE Select	ENSP00000352540.3:n.170-1174_170-1170delinsGAAAA
ENST00000359543.7:c.170-1174_170-1170delinsGAAAA	ENSP00000352540.3:n.170-1174_170-1170delinsGAAAA
ENST00000536829.1:c.170-1174_170-1170delinsGAAAA	ENSP00000445712.1:n.170-1174_170-1170delinsGAAAA
NM_001424.4:c.170-1174_170-1170delinsGAAAA	NP_001415.1:n.170-1174_170-1170delinsGAAAA
NM_001424.5:c.170-1174_170-1170delinsGAAAA	NP_001415.1:n.170-1174_170-1170delinsGAAAA
XM_006720864.2:c.170-1174_170-1170delinsGAAAA	XP_006720927.1:n.170-1174_170-1170delinsGAAAA
XM_006720864.3:c.170-1174_170-1170delinsGAAAA	XP_006720927.1:n.170-1174_170-1170delinsGAAAA
NM_001424.6:c.170-1174_170-1170delinsGAAAA MANE Select	NP_001415.1:n.170-1174_170-1170delinsGAAAA