Canonical Allele Identifier: CA1700400393

Gene: ELMO1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.37037296_37037299delinsCGTT , CM000669.2:g.37037296_37037299delinsCGTT	GRCh38
NC_000007.13:g.37076901_37076904delinsCGTT , CM000669.1:g.37076901_37076904delinsCGTT	GRCh37
NC_000007.12:g.37043426_37043429delinsCGTT	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000310758.9:c.1301-23864_1301-23861delinsAACG MANE Select	ENSP00000312185.4:n.1301-23864_1301-23861...
ENST00000310758.8:c.1301-23864_1301-23861delinsAACG	ENSP00000312185.4:n.1301-23864_1301-23861...
ENST00000420636.5:c.515-3887_515-3884delinsAACG	ENSP00000396465.1:n.515-3887_515-3884deli...
ENST00000442504.5:c.1301-23864_1301-23861delinsAACG	ENSP00000406952.1:n.1301-23864_1301-23861...
ENST00000448602.5:c.1301-23864_1301-23861delinsAACG	ENSP00000394458.1:n.1301-23864_1301-23861...
ENST00000472359.1:n.338-23864_338-23861delinsAACG
NM_001206480.2:c.1301-23864_1301-23861delinsAACG	NP_001193409.1:n.1301-23864_1301-23861del...
NM_001206482.1:c.1301-23864_1301-23861delinsAACG	NP_001193411.1:n.1301-23864_1301-23861del...
NM_014800.10:c.1301-23864_1301-23861delinsAACG	NP_055615.8:n.1301-23864_1301-23861delins...
XM_005249919.1:c.1301-23864_1301-23861delinsAACG	XP_005249976.1:n.1301-23864_1301-23861del...
XM_006715805.1:c.1301-23864_1301-23861delinsAACG	XP_006715868.1:n.1301-23864_1301-23861del...
XM_011515654.1:c.1301-23864_1301-23861delinsAACG	XP_011513956.1:n.1301-23864_1301-23861del...
XM_011515655.1:c.1301-23864_1301-23861delinsAACG	XP_011513957.1:n.1301-23864_1301-23861del...
XM_005249919.3:c.1301-23864_1301-23861delinsAACG	XP_005249976.1:n.1301-23864_1301-23861del...
XM_011515654.2:c.1301-23864_1301-23861delinsAACG	XP_011513956.1:n.1301-23864_1301-23861del...
XM_017012839.1:c.1301-23864_1301-23861delinsAACG	XP_016868328.1:n.1301-23864_1301-23861del...
XM_024447008.1:c.1301-23864_1301-23861delinsAACG	XP_024302776.1:n.1301-23864_1301-23861del...
XR_001744894.2:n.1650-23864_1650-23861delinsAACG
NM_001206482.2:c.1301-23864_1301-23861delinsAACG	NP_001193411.1:n.1301-23864_1301-23861del...
NM_014800.11:c.1301-23864_1301-23861delinsAACG MANE Select	NP_055615.8:n.1301-23864_1301-23861delins...