Canonical Allele Identifier: CA1700341223

Gene: ELMO1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.36903663C= , CM000669.2:g.36903663C=	GRCh38
NC_000007.13:g.36943268C= , CM000669.1:g.36943268C=	GRCh37
NC_000007.12:g.36909793C=	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000310758.9:c.1438-8646G= MANE Select	ENSP00000312185.4:n.1438-8646G=
ENST00000310758.8:c.1438-8646G=	ENSP00000312185.4:n.1438-8646G=
ENST00000396040.6:c.-3-8646G=	ENSP00000379355.2:n.-3-8646G=
ENST00000396045.7:c.-3-8646G=	ENSP00000379360.3:n.-3-8646G=
ENST00000420636.5:c.718-8646G=	ENSP00000396465.1:n.718-8646G=
ENST00000442504.5:c.1438-8646G=	ENSP00000406952.1:n.1438-8646G=
ENST00000448602.5:c.1438-8646G=	ENSP00000394458.1:n.1438-8646G=
ENST00000464262.6:n.195-8646G=
ENST00000472359.1:n.475-8646G=
ENST00000487843.1:n.228-8646G=
NM_001039459.2:c.-3-8646G=	NP_001034548.1:n.-3-8646G=
NM_001206480.2:c.1438-8646G=	NP_001193409.1:n.1438-8646G=
NM_001206482.1:c.1438-8646G=	NP_001193411.1:n.1438-8646G=
NM_014800.10:c.1438-8646G=	NP_055615.8:n.1438-8646G=
NM_130442.3:c.-3-8646G=	NP_569709.1:n.-3-8646G=
NR_038120.1:n.345-8646G=
XM_005249919.1:c.1438-8646G=	XP_005249976.1:n.1438-8646G=
XM_006715805.1:c.1438-8646G=	XP_006715868.1:n.1438-8646G=
XM_011515654.1:c.1438-8646G=	XP_011513956.1:n.1438-8646G=
XM_011515655.1:c.1438-8646G=	XP_011513957.1:n.1438-8646G=
XM_005249919.3:c.1438-8646G=	XP_005249976.1:n.1438-8646G=
XM_011515654.2:c.1438-8646G=	XP_011513956.1:n.1438-8646G=
XM_017012839.1:c.1438-8646G=	XP_016868328.1:n.1438-8646G=
XM_024447008.1:c.1438-8646G=	XP_024302776.1:n.1438-8646G=
XR_001744894.2:n.1787-8646G=
NM_001039459.3:c.-3-8646G=	NP_001034548.1:n.-3-8646G=
NM_001206482.2:c.1438-8646G=	NP_001193411.1:n.1438-8646G=
NM_014800.11:c.1438-8646G= MANE Select	NP_055615.8:n.1438-8646G=
NM_130442.4:c.-3-8646G=	NP_569709.1:n.-3-8646G=
NR_038120.2:n.212-8646G=