Canonical Allele Identifier: CA2207124548
Gene: EMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10539333G= , CM000678.2:g.10539333G= GRCh38
NC_000016.9:g.10633190G= , CM000678.1:g.10633190G= GRCh37
NC_000016.8:g.10540691G= NCBI36
NG_042058.1:g.46384C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359543.8:c.170-1259C= MANE Select ENSP00000352540.3:n.170-1259C=
ENST00000359543.7:c.170-1259C= ENSP00000352540.3:n.170-1259C=
ENST00000536829.1:c.170-1259C= ENSP00000445712.1:n.170-1259C=
NM_001424.4:c.170-1259C= NP_001415.1:n.170-1259C=
NM_001424.5:c.170-1259C= NP_001415.1:n.170-1259C=
XM_006720864.2:c.170-1259C= XP_006720927.1:n.170-1259C=
XM_006720864.3:c.170-1259C= XP_006720927.1:n.170-1259C=
NM_001424.6:c.170-1259C= MANE Select NP_001415.1:n.170-1259C=