Canonical Allele Identifier: CA2207124386

Gene: EMP2

Linked Data

• dbSNP Id: rs2050673908

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10539081_10539085del , CM000678.2:g.10539081_10539085del	GRCh38
NC_000016.9:g.10632938_10632942del , CM000678.1:g.10632938_10632942del	GRCh37
NC_000016.8:g.10540439_10540443del	NCBI36
NG_042058.1:g.46635_46639del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359543.8:c.170-1008_170-1004del MANE Select	ENSP00000352540.3:n.170-1008_170-1004del
ENST00000359543.7:c.170-1008_170-1004del	ENSP00000352540.3:n.170-1008_170-1004del
ENST00000536829.1:c.170-1008_170-1004del	ENSP00000445712.1:n.170-1008_170-1004del
NM_001424.4:c.170-1008_170-1004del	NP_001415.1:n.170-1008_170-1004del
NM_001424.5:c.170-1008_170-1004del	NP_001415.1:n.170-1008_170-1004del
XM_006720864.2:c.170-1008_170-1004del	XP_006720927.1:n.170-1008_170-1004del
XM_006720864.3:c.170-1008_170-1004del	XP_006720927.1:n.170-1008_170-1004del
NM_001424.6:c.170-1008_170-1004del MANE Select	NP_001415.1:n.170-1008_170-1004del