Canonical Allele Identifier: CA974612288

Gene: EMP2

Linked Data

• gnomAD v3: 16-10539178-A-ATTTTTT
• gnomAD v4: 16-10539178-A-ATTTTTT

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10539178_10539179insTTTTTT , CM000678.2:g.10539178_10539179insTTTTTT	GRCh38
NC_000016.9:g.10633035_10633036insTTTTTT , CM000678.1:g.10633035_10633036insTTTTTT	GRCh37
NC_000016.8:g.10540536_10540537insTTTTTT	NCBI36
NG_042058.1:g.46538_46539insAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359543.8:c.170-1105_170-1104insAAAAAA MANE Select	ENSP00000352540.3:n.170-1105_170-1104insAAAAAA
ENST00000359543.7:c.170-1105_170-1104insAAAAAA	ENSP00000352540.3:n.170-1105_170-1104insAAAAAA
ENST00000536829.1:c.170-1105_170-1104insAAAAAA	ENSP00000445712.1:n.170-1105_170-1104insAAAAAA
NM_001424.4:c.170-1105_170-1104insAAAAAA	NP_001415.1:n.170-1105_170-1104insAAAAAA
NM_001424.5:c.170-1105_170-1104insAAAAAA	NP_001415.1:n.170-1105_170-1104insAAAAAA
XM_006720864.2:c.170-1105_170-1104insAAAAAA	XP_006720927.1:n.170-1105_170-1104insAAAAAA
XM_006720864.3:c.170-1105_170-1104insAAAAAA	XP_006720927.1:n.170-1105_170-1104insAAAAAA
NM_001424.6:c.170-1105_170-1104insAAAAAA MANE Select	NP_001415.1:n.170-1105_170-1104insAAAAAA