Canonical Allele Identifier: CA920253368
Gene: EEF1A2 HGNC NCBI

Linked Data

dbSNP Id: rs1600908592

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.63496037_63496038insCAGCAGCCTCCTTCTCGAATTTCT , CM000682.2:g.63496037_63496038insCAGCAGCCTCCTTCTCGAATTTCT GRCh38
NC_000020.10:g.62127390_62127391insCAGCAGCCTCCTTCTCGAATTTCT , CM000682.1:g.62127390_62127391insCAGCAGCCTCCTTCTCGAATTTCT GRCh37
NC_000020.9:g.61597834_61597835insCAGCAGCCTCCTTCTCGAATTTCT NCBI36
NG_034083.1:g.8281_8282insAATTCGAGAAGGAGGCTGCTGAGA

Transcript Alleles

HGVS Amino-acid Change
ENST00000706948.1:c.145_146insAATTCGAGAAGGAGGCTGCTGAGA
ENST00000706949.1:c.145_146insAATTCGAGAAGGAGGCTGCTGAGA
ENST00000217182.6:c.145_146insAATTCGAGAAGGAGGCTGCTGAGA
ENST00000298049.12:c.145_146insAATTCGAGAAGGAGGCTGCTGAGA
ENST00000642899.1:c.145_146insAATTCGAGAAGGAGGCTGCTGAGA
ENST00000645357.1:c.145_146insAATTCGAGAAGGAGGCTGCTGAGA
ENST00000645586.1:n.2714_2715insAATTCGAGAAGGAGGCTGCTGAGA
ENST00000646335.1:c.145_146insAATTCGAGAAGGAGGCTGCTGAGA
ENST00000675519.1:c.*17_*18insAATTCGAGAAGGAGGCTGCTGAGA ENSP00000501859.1:n.*17_*18insAATTCGAGAAGGAGGCTGCTGAGA
ENST00000217182.4:c.145_146insAATTCGAGAAGGAGGCTGCTGAGA
ENST00000298049.11:c.145_146insAATTCGAGAAGGAGGCTGCTGAGA
NM_001958.3:c.145_146insAATTCGAGAAGGAGGCTGCTGAGA
NM_001958.4:c.145_146insAATTCGAGAAGGAGGCTGCTGAGA
NM_001958.5:c.145_146insAATTCGAGAAGGAGGCTGCTGAGA