Canonical Allele Identifier: CA2207124311
Gene: EMP2 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10538933A= , CM000678.2:g.10538933A= GRCh38
NC_000016.9:g.10632790A= , CM000678.1:g.10632790A= GRCh37
NC_000016.8:g.10540291A= NCBI36
NG_042058.1:g.46784T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000359543.8:c.170-859T= MANE Select ENSP00000352540.3:n.170-859T=
ENST00000359543.7:c.170-859T= ENSP00000352540.3:n.170-859T=
ENST00000536829.1:c.170-859T= ENSP00000445712.1:n.170-859T=
NM_001424.4:c.170-859T= NP_001415.1:n.170-859T=
NM_001424.5:c.170-859T= NP_001415.1:n.170-859T=
XM_006720864.2:c.170-859T= XP_006720927.1:n.170-859T=
XM_006720864.3:c.170-859T= XP_006720927.1:n.170-859T=
NM_001424.6:c.170-859T= MANE Select NP_001415.1:n.170-859T=
Search 100 bp 5'
Search 100 bp 3'