Canonical Allele Identifier: CA14239887

Gene: EMP2

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.10539308A>G , CM000678.2:g.10539308A>G	GRCh38
NC_000016.9:g.10633165A>G , CM000678.1:g.10633165A>G	GRCh37
NC_000016.8:g.10540666A>G	NCBI36
NG_042058.1:g.46409T>C

Transcript Alleles

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