Canonical Allele Identifier: CA2653148578

Gene: ELMO2

Linked Data

• gnomAD v4: 20-46375141-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000020.11:g.46375141C>A , CM000682.2:g.46375141C>A	GRCh38
NC_000020.10:g.45003780C>A , CM000682.1:g.45003780C>A	GRCh37
NC_000020.9:g.44437187C>A	NCBI36
NG_053169.1:g.36911G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000290246.11:c.1065+95G>T MANE Select	ENSP00000290246.6:n.1065+95G>T
ENST00000290246.10:c.1065+95G>T	ENSP00000290246.6:n.1065+95G>T
ENST00000352077.6:c.1059+95G>T	ENSP00000326172.4:n.1059+95G>T
ENST00000372176.5:c.801+95G>T	ENSP00000361249.1:n.801+95G>T
ENST00000396391.5:c.1065+95G>T	ENSP00000379673.1:n.1065+95G>T
ENST00000425546.5:c.429+95G>T	ENSP00000388962.1:n.429+95G>T
ENST00000462491.5:n.429+95G>T
ENST00000467800.5:c.239+95G>T
ENST00000481852.5:n.522+95G>T
ENST00000488853.5:n.1142+95G>T
NM_133171.3:c.1065+95G>T	NP_573403.1:n.1065+95G>T
NM_182764.1:c.1065+95G>T	NP_877496.1:n.1065+95G>T
XM_005260496.2:c.1065+95G>T	XP_005260553.1:n.1065+95G>T
XM_005260497.2:c.801+95G>T	XP_005260554.1:n.801+95G>T
XM_005260498.2:c.801+95G>T	XP_005260555.1:n.801+95G>T
XM_005260499.2:c.801+95G>T	XP_005260556.1:n.801+95G>T
XM_005260500.2:c.801+95G>T	XP_005260557.1:n.801+95G>T
XM_005260501.3:c.516+95G>T	XP_005260558.1:n.516+95G>T
XM_005260502.3:c.516+95G>T	XP_005260559.1:n.516+95G>T
XM_006723854.2:c.1065+95G>T	XP_006723917.1:n.1065+95G>T
NM_001318253.1:c.801+95G>T	NP_001305182.1:n.801+95G>T
NM_133171.4:c.1065+95G>T	NP_573403.1:n.1065+95G>T
NM_182764.2:c.1065+95G>T	NP_877496.1:n.1065+95G>T
XM_005260496.3:c.1065+95G>T	XP_005260553.1:n.1065+95G>T
XM_005260498.3:c.801+95G>T	XP_005260555.1:n.801+95G>T
XM_005260499.3:c.801+95G>T	XP_005260556.1:n.801+95G>T
XM_005260500.3:c.801+95G>T	XP_005260557.1:n.801+95G>T
XM_005260501.5:c.516+95G>T	XP_005260558.1:n.516+95G>T
XM_006723854.3:c.1065+95G>T	XP_006723917.1:n.1065+95G>T
XM_017028009.1:c.516+95G>T	XP_016883498.1:n.516+95G>T
XM_017028010.1:c.516+95G>T	XP_016883499.1:n.516+95G>T
XM_017028011.1:c.516+95G>T	XP_016883500.1:n.516+95G>T
XM_024451961.1:c.516+95G>T	XP_024307729.1:n.516+95G>T
NM_133171.5:c.1065+95G>T MANE Select	NP_573403.1:n.1065+95G>T
NM_001318253.2:c.801+95G>T	NP_001305182.1:n.801+95G>T
NM_182764.3:c.1065+95G>T	NP_877496.1:n.1065+95G>T