Canonical Allele Identifier: CA2458270116
Gene: ELF4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.130065773_130065777delinsCAAAT , CM000685.2:g.130065773_130065777delinsCAAAT GRCh38
NC_000023.10:g.129199748_129199752delinsCAAAT , CM000685.1:g.129199748_129199752delinsCAAAT GRCh37
NC_000023.9:g.129027429_129027433delinsCAAAT NCBI36
NG_016388.1:g.49937_49941delinsATTTG , LRG_335:g.49937_49941delinsATTTG

Transcript Alleles

HGVS Amino-acid Change
ENST00000308167.10:c.*944_*948delinsATTTG MANE Select ENSP00000311280.6:n.*944_*948delinsATTTG
ENST00000308167.9:c.*944_*948delinsATTTG ENSP00000311280.5:n.*944_*948delinsATTTG
ENST00000335997.11:c.*944_*948delinsATTTG ENSP00000338608.7:n.*944_*948delinsATTTG
ENST00000615377.4:c.*944_*948delinsATTTG ENSP00000478297.1:n.*944_*948delinsATTTG
NM_001127197.1:c.*944_*948delinsATTTG NP_001120669.1:n.*944_*948delinsATTTG
NM_001421.3:c.*944_*948delinsATTTG , LRG_335t1:c.*944_*948delinsATTTG NP_001412.1:n.*944_*948delinsATTTG
XM_005262389.2:c.*944_*948delinsATTTG XP_005262446.1:n.*944_*948delinsATTTG
XM_011531307.1:c.*944_*948delinsATTTG XP_011529609.1:n.*944_*948delinsATTTG
XM_011531308.1:c.*944_*948delinsATTTG XP_011529610.1:n.*944_*948delinsATTTG
XM_005262389.3:c.*944_*948delinsATTTG XP_005262446.1:n.*944_*948delinsATTTG
XM_011531307.3:c.*944_*948delinsATTTG XP_011529609.1:n.*944_*948delinsATTTG
XM_011531308.3:c.*944_*948delinsATTTG XP_011529610.1:n.*944_*948delinsATTTG
NM_001127197.2:c.*944_*948delinsATTTG NP_001120669.1:n.*944_*948delinsATTTG
NM_001421.4:c.*944_*948delinsATTTG MANE Select NP_001412.1:n.*944_*948delinsATTTG