Canonical Allele Identifier: CA2207124559
Gene: EMP2 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10539365A= , CM000678.2:g.10539365A= GRCh38
NC_000016.9:g.10633222A= , CM000678.1:g.10633222A= GRCh37
NC_000016.8:g.10540723A= NCBI36
NG_042058.1:g.46352T=

Transcript Alleles

HGVS Amino-acid change
ENST00000359543.8:c.170-1291T= MANE Select ENSP00000352540.3:n.170-1291T=
ENST00000359543.7:c.170-1291T= ENSP00000352540.3:n.170-1291T=
ENST00000536829.1:c.170-1291T= ENSP00000445712.1:n.170-1291T=
NM_001424.4:c.170-1291T= NP_001415.1:n.170-1291T=
NM_001424.5:c.170-1291T= NP_001415.1:n.170-1291T=
XM_006720864.2:c.170-1291T= XP_006720927.1:n.170-1291T=
XM_006720864.3:c.170-1291T= XP_006720927.1:n.170-1291T=
NM_001424.6:c.170-1291T= MANE Select NP_001415.1:n.170-1291T=
Search 100 bp 5'
Search 100 bp 3'