Canonical Allele Identifier: CA2510050224
Gene: EMP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.10538943G>A , CM000678.2:g.10538943G>A GRCh38
NC_000016.9:g.10632800G>A , CM000678.1:g.10632800G>A GRCh37
NC_000016.8:g.10540301G>A NCBI36
NG_042058.1:g.46774C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000359543.8:c.170-869C>T MANE Select ENSP00000352540.3:n.170-869C>T
ENST00000359543.7:c.170-869C>T ENSP00000352540.3:n.170-869C>T
ENST00000536829.1:c.170-869C>T ENSP00000445712.1:n.170-869C>T
NM_001424.4:c.170-869C>T NP_001415.1:n.170-869C>T
NM_001424.5:c.170-869C>T NP_001415.1:n.170-869C>T
XM_006720864.2:c.170-869C>T XP_006720927.1:n.170-869C>T
XM_006720864.3:c.170-869C>T XP_006720927.1:n.170-869C>T
NM_001424.6:c.170-869C>T MANE Select NP_001415.1:n.170-869C>T