Canonical Allele Identifier: CA277624339

Gene: EMP2

Linked Data

• dbSNP Id: rs386788904

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10539307_10539308delinsTG , CM000678.2:g.10539307_10539308delinsTG	GRCh38
NC_000016.9:g.10633164_10633165delinsTG , CM000678.1:g.10633164_10633165delinsTG	GRCh37
NC_000016.8:g.10540665_10540666delinsTG	NCBI36
NG_042058.1:g.46409_46410delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359543.8:c.170-1234_170-1233delinsCA MANE Select	ENSP00000352540.3:n.170-1234_170-1233delinsCA
ENST00000359543.7:c.170-1234_170-1233delinsCA	ENSP00000352540.3:n.170-1234_170-1233delinsCA
ENST00000536829.1:c.170-1234_170-1233delinsCA	ENSP00000445712.1:n.170-1234_170-1233delinsCA
NM_001424.4:c.170-1234_170-1233delinsCA	NP_001415.1:n.170-1234_170-1233delinsCA
NM_001424.5:c.170-1234_170-1233delinsCA	NP_001415.1:n.170-1234_170-1233delinsCA
XM_006720864.2:c.170-1234_170-1233delinsCA	XP_006720927.1:n.170-1234_170-1233delinsCA
XM_006720864.3:c.170-1234_170-1233delinsCA	XP_006720927.1:n.170-1234_170-1233delinsCA
NM_001424.6:c.170-1234_170-1233delinsCA MANE Select	NP_001415.1:n.170-1234_170-1233delinsCA