Canonical Allele Identifier: CA9890085

Gene: ELMO2

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46373390G>C , CM000682.2:g.46373390G>C	GRCh38
NC_000020.10:g.45002029G>C , CM000682.1:g.45002029G>C	GRCh37
NC_000020.9:g.44435436G>C	NCBI36
NG_053169.1:g.38662C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000290246.11:c.1416+9C>G MANE Select	ENSP00000290246.6:n.1416+9C>G
ENST00000290246.10:c.1416+9C>G	ENSP00000290246.6:n.1416+9C>G
ENST00000352077.6:c.1410+9C>G	ENSP00000326172.4:n.1410+9C>G
ENST00000372176.5:c.1152+9C>G	ENSP00000361249.1:n.1152+9C>G
ENST00000396391.5:c.1416+9C>G	ENSP00000379673.1:n.1416+9C>G
ENST00000425546.5:c.789C>G	ENSP00000388962.1:p.Val263=
ENST00000452857.5:c.117+9C>G	ENSP00000414329.1:n.117+9C>G
ENST00000462491.5:n.789C>G
ENST00000464448.1:n.97+9C>G
ENST00000467800.5:c.590+9C>G
NM_133171.3:c.1416+9C>G	NP_573403.1:n.1416+9C>G
NM_182764.1:c.1416+9C>G	NP_877496.1:n.1416+9C>G
XM_005260496.2:c.1416+9C>G	XP_005260553.1:n.1416+9C>G
XM_005260497.2:c.1152+9C>G	XP_005260554.1:n.1152+9C>G
XM_005260498.2:c.1152+9C>G	XP_005260555.1:n.1152+9C>G
XM_005260499.2:c.1152+9C>G	XP_005260556.1:n.1152+9C>G
XM_005260500.2:c.1152+9C>G	XP_005260557.1:n.1152+9C>G
XM_005260501.3:c.867+9C>G	XP_005260558.1:n.867+9C>G
XM_005260502.3:c.867+9C>G	XP_005260559.1:n.867+9C>G
XM_006723854.2:c.1416+9C>G	XP_006723917.1:n.1416+9C>G
NM_001318253.1:c.1152+9C>G	NP_001305182.1:n.1152+9C>G
NM_133171.4:c.1416+9C>G	NP_573403.1:n.1416+9C>G
NM_182764.2:c.1416+9C>G	NP_877496.1:n.1416+9C>G
XM_005260496.3:c.1416+9C>G	XP_005260553.1:n.1416+9C>G
XM_005260498.3:c.1152+9C>G	XP_005260555.1:n.1152+9C>G
XM_005260499.3:c.1152+9C>G	XP_005260556.1:n.1152+9C>G
XM_005260500.3:c.1152+9C>G	XP_005260557.1:n.1152+9C>G
XM_005260501.5:c.867+9C>G	XP_005260558.1:n.867+9C>G
XM_006723854.3:c.1416+9C>G	XP_006723917.1:n.1416+9C>G
XM_017028009.1:c.867+9C>G	XP_016883498.1:n.867+9C>G
XM_017028010.1:c.867+9C>G	XP_016883499.1:n.867+9C>G
XM_017028011.1:c.867+9C>G	XP_016883500.1:n.867+9C>G
XM_024451961.1:c.867+9C>G	XP_024307729.1:n.867+9C>G
NM_133171.5:c.1416+9C>G MANE Select	NP_573403.1:n.1416+9C>G
NM_001318253.2:c.1152+9C>G	NP_001305182.1:n.1152+9C>G
NM_182764.3:c.1416+9C>G	NP_877496.1:n.1416+9C>G