Canonical Allele Identifier: CA461551320

Gene: ELOC

Linked Data

• MyVariant Identifiers: chr8:g.74859033G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.73946798G>C , CM000670.2:g.73946798G>C	GRCh38
NC_000008.10:g.74859033G>C , CM000670.1:g.74859033G>C	GRCh37
NC_000008.9:g.75021587G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000519487.6:c.240C>G	ENSP00000429596.2:p.Thr80=
ENST00000622804.2:c.171C>G	ENSP00000478121.1:p.Thr57=
ENST00000685250.1:n.279C>G
ENST00000685938.1:c.234C>G	ENSP00000509885.1:p.Thr78=
ENST00000687224.1:c.171C>G	ENSP00000509184.1:p.Thr57=
ENST00000688584.1:c.123C>G	ENSP00000509989.1:p.Thr41=
ENST00000692141.1:n.4245C>G
ENST00000520242.6:c.171C>G MANE Select	ENSP00000428171.1:p.Thr57=
ENST00000284811.12:c.171C>G	ENSP00000284811.8:p.Thr57=
ENST00000518127.5:c.171C>G	ENSP00000428334.1:p.Thr57=
ENST00000519082.5:c.171C>G	ENSP00000429789.1:p.Thr57=
ENST00000519487.5:c.171C>G	ENSP00000429596.1:p.Thr57=
ENST00000520210.1:c.123C>G	ENSP00000430224.1:p.Thr41=
ENST00000520242.5:c.171C>G	ENSP00000428171.1:p.Thr57=
ENST00000522337.5:c.171C>G	ENSP00000429906.1:p.Thr57=
ENST00000523815.5:c.171C>G	ENSP00000428074.1:p.Thr57=
ENST00000602840.5:c.149-5193C>G	ENSP00000473408.1:n.149-5193C>G
ENST00000622804.1:c.171C>G	ENSP00000478121.1:p.Thr57=
NM_001204857.1:c.171C>G	NP_001191786.1:p.Thr57=
NM_001204858.1:c.171C>G	NP_001191787.1:p.Thr57=
NM_001204859.1:c.171C>G	NP_001191788.1:p.Thr57=
NM_001204860.1:c.171C>G	NP_001191789.1:p.Thr57=
NM_001204861.1:c.171C>G	NP_001191790.1:p.Thr57=
NM_001204862.1:c.171C>G	NP_001191791.1:p.Thr57=
NM_001204863.1:c.123C>G	NP_001191792.1:p.Thr41=
NM_001204864.1:c.123C>G	NP_001191793.1:p.Thr41=
NM_005648.3:c.171C>G	NP_005639.1:p.Thr57=
XM_011517580.1:c.171C>G	XP_011515882.1:p.Thr57=
XM_011517581.1:c.171C>G	XP_011515883.1:p.Thr57=
XM_011517580.2:c.171C>G	XP_011515882.1:p.Thr57=
XM_011517581.2:c.171C>G	XP_011515883.1:p.Thr57=
NM_001204858.2:c.171C>G	NP_001191787.1:p.Thr57=
NM_001204859.2:c.171C>G	NP_001191788.1:p.Thr57=
NM_001204863.2:c.123C>G	NP_001191792.1:p.Thr41=
NM_005648.4:c.171C>G MANE Select	NP_005639.1:p.Thr57=
NM_001204857.2:c.171C>G	NP_001191786.1:p.Thr57=
NM_001204860.2:c.171C>G	NP_001191789.1:p.Thr57=
NM_001204861.2:c.171C>G	NP_001191790.1:p.Thr57=
NM_001204862.2:c.171C>G	NP_001191791.1:p.Thr57=
NM_001204864.2:c.123C>G	NP_001191793.1:p.Thr41=