Canonical Allele Identifier: CA3155852528
Community Standard Title: NM_014800.11(ELMO1):c.832-1542G>A
Gene: ELMO1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37214999C>T , CM000669.2:g.37214999C>T GRCh38
NC_000007.13:g.37254604C>T , CM000669.1:g.37254604C>T GRCh37
NC_000007.12:g.37221129C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_014800.11:c.832-1542G>A MANE Select NP_055615.8:n.832-1542G>A
ENST00000310758.9:c.832-1542G>A MANE Select ENSP00000312185.4:n.832-1542G>A
NM_001206480.2:c.832-1542G>A NP_001193409.1:n.832-1542G>A
NM_001206482.1:c.832-1542G>A NP_001193411.1:n.832-1542G>A
NM_001206482.2:c.832-1542G>A NP_001193411.1:n.832-1542G>A
NM_014800.10:c.832-1542G>A NP_055615.8:n.832-1542G>A
ENST00000310758.8:c.832-1542G>A ENSP00000312185.4:n.832-1542G>A
ENST00000420636.5:c.46-1542G>A ENSP00000396465.1:n.46-1542G>A
ENST00000424212.1:c.55-1542G>A ENSP00000395933.1:n.55-1542G>A
ENST00000433246.5:c.171-1542G>A
ENST00000442504.5:c.832-1542G>A ENSP00000406952.1:n.832-1542G>A
ENST00000448602.5:c.832-1542G>A ENSP00000394458.1:n.832-1542G>A
ENST00000487336.1:n.172-1542G>A
XM_005249919.1:c.832-1542G>A XP_005249976.1:n.832-1542G>A
XM_005249919.3:c.832-1542G>A XP_005249976.1:n.832-1542G>A
XM_006715805.1:c.832-1542G>A XP_006715868.1:n.832-1542G>A
XM_011515654.1:c.832-1542G>A XP_011513956.1:n.832-1542G>A
XM_011515654.2:c.832-1542G>A XP_011513956.1:n.832-1542G>A
XM_011515655.1:c.832-1542G>A XP_011513957.1:n.832-1542G>A
XM_017012839.1:c.832-1542G>A XP_016868328.1:n.832-1542G>A
XM_024447008.1:c.832-1542G>A XP_024302776.1:n.832-1542G>A
XR_001744894.2:n.1181-1542G>A