Canonical Allele Identifier: CA717886406

Gene: EMP2

Linked Data

• dbSNP Id: rs1190978266
• MyVariant Identifiers: chr16:g.10633089_10633093del (hg19) ; chr16:g.10539232_10539236del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10539233_10539237del , CM000678.2:g.10539233_10539237del	GRCh38
NC_000016.9:g.10633090_10633094del , CM000678.1:g.10633090_10633094del	GRCh37
NC_000016.8:g.10540591_10540595del	NCBI36
NG_042058.1:g.46481_46485del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000359543.8:c.170-1162_170-1158del MANE Select	ENSP00000352540.3:n.170-1162_170-1158del
ENST00000359543.7:c.170-1162_170-1158del	ENSP00000352540.3:n.170-1162_170-1158del
ENST00000536829.1:c.170-1162_170-1158del	ENSP00000445712.1:n.170-1162_170-1158del
NM_001424.4:c.170-1162_170-1158del	NP_001415.1:n.170-1162_170-1158del
NM_001424.5:c.170-1162_170-1158del	NP_001415.1:n.170-1162_170-1158del
XM_006720864.2:c.170-1162_170-1158del	XP_006720927.1:n.170-1162_170-1158del
XM_006720864.3:c.170-1162_170-1158del	XP_006720927.1:n.170-1162_170-1158del
NM_001424.6:c.170-1162_170-1158del MANE Select	NP_001415.1:n.170-1162_170-1158del