Canonical Allele Identifier: CA974612140

Gene: EMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10538942T>A , CM000678.2:g.10538942T>A	GRCh38
NC_000016.9:g.10632799T>A , CM000678.1:g.10632799T>A	GRCh37
NC_000016.8:g.10540300T>A	NCBI36
NG_042058.1:g.46775A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359543.8:c.170-868A>T MANE Select	ENSP00000352540.3:n.170-868A>T
ENST00000359543.7:c.170-868A>T	ENSP00000352540.3:n.170-868A>T
ENST00000536829.1:c.170-868A>T	ENSP00000445712.1:n.170-868A>T
NM_001424.4:c.170-868A>T	NP_001415.1:n.170-868A>T
NM_001424.5:c.170-868A>T	NP_001415.1:n.170-868A>T
XM_006720864.2:c.170-868A>T	XP_006720927.1:n.170-868A>T
XM_006720864.3:c.170-868A>T	XP_006720927.1:n.170-868A>T
NM_001424.6:c.170-868A>T MANE Select	NP_001415.1:n.170-868A>T