Canonical Allele Identifier: CA2207124533

Gene: EMP2

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10539307_10539308delinsCA , CM000678.2:g.10539307_10539308delinsCA	GRCh38
NC_000016.9:g.10633164_10633165delinsCA , CM000678.1:g.10633164_10633165delinsCA	GRCh37
NC_000016.8:g.10540665_10540666delinsCA	NCBI36
NG_042058.1:g.46409_46410delinsTG

Transcript Alleles

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