Canonical Allele Identifier: CA1700565859

Gene: ELMO1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.37397251A= , CM000669.2:g.37397251A=	GRCh38
NC_000007.13:g.37436854A= , CM000669.1:g.37436854A=	GRCh37
NC_000007.12:g.37403379A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000310758.9:c.-74+51424T= MANE Select	ENSP00000312185.4:n.-74+51424T=
ENST00000310758.8:c.-74+51424T=	ENSP00000312185.4:n.-74+51424T=
ENST00000445322.1:c.-169-3334T=	ENSP00000397857.1:n.-169-3334T=
ENST00000448602.5:c.-74+51609T=	ENSP00000394458.1:n.-74+51609T=
ENST00000453399.5:c.-169-3334T=	ENSP00000391734.1:n.-169-3334T=
ENST00000463390.1:n.182+51424T=
NM_001206480.2:c.-74+51609T=	NP_001193409.1:n.-74+51609T=
NM_014800.10:c.-74+51424T=	NP_055615.8:n.-74+51424T=
XM_011515654.1:c.-74+31540T=	XP_011513956.1:n.-74+31540T=
XM_011515655.1:c.-74+51424T=	XP_011513957.1:n.-74+51424T=
XM_005249919.3:c.-169-3334T=	XP_005249976.1:n.-169-3334T=
XM_011515654.2:c.-74+31540T=	XP_011513956.1:n.-74+31540T=
XR_001744894.2:n.276+51424T=
NM_014800.11:c.-74+51424T= MANE Select	NP_055615.8:n.-74+51424T=